Molecular melt and methods for making and using the molecular melt

ABSTRACT

The present invention includes a molecular melt composition comprising an antioxidant and a modifying agent. The molecular melt is partially amorphous in nature. The invention also includes a method for making the molecular melt composition and a method for using the molecular melt to produce modified polymers. The invention further includes a method for using an antioxidant to phlagmatize a modifying agent.

CROSS REFERENCE STATEMENT

[0001] This application claims benefit from U.S. Provisional Application No. 60/335,224 filed Nov. 2, 2001.

BACKGROUND

[0002] Polyolefins and other polymers are frequently modified in order to improve their rheological and other physical properties. Various chemical agents have been used to carry out such modifications.

[0003] One method for modifying polymers, such as polyolefins, is to use molecules that are capable of providing a nitrene reactive group(s) for insertion into C—H bonds on the polymers. An example of such a class of chemicals are the sulfonyl azides which are disclosed in WO 99/10424 published Mar. 4, 1999, which is hereby incorporated by reference for its teachings regarding azides. When heated to an appropriate reaction temperature, these azides decompose to form nitrene groups that can then insert into C—H bonds on the polymers. These sulfonyl azides are effective for providing nitrene groups for insertion into the C—H bonds of styrenic based and polyolefin based polymers.

[0004] However, sulfonyl azides and other azides can be shock sensitive. It may be necessary to phlagmatize the azides or to otherwise protect the azides from reaction during the manufacture and processing of the azide and the shipping and handling of the azide. However, the methods that would typically be used to protect chemicals such as azides from reacting can be expensive and may not be compatible with the polymers that are to be modified. Additionally, polymers are often used for packaging food. Therefore, it is important that the addition of the protective agent not prevent the modified polymer from being approved for food packaging applications.

[0005] What is desired is a relatively inexpensive and easy manner for phlagmatizing a coupling agent that also does not interfere with the coupling agent or limit the use of the, coupling agent for producing modified polymers.

[0006] As used herein, the following terms shall have the following meanings:

[0007] (a) “Coupling Agent” shall mean a chemical compound that contains at least two reactive groups that are each capable of forming a carbene or nitrene group that are capable of inserting into the carbon hydrogen bonds of CH, CH2, or CH3 groups, both aliphatic and/or aromatic, of a polymer chain. The reactive groups together can couple or cross-link polymer chains. It may be necessary to activate a coupling agent with heat, sonic energy, radiation or other chemical activating energy, for the coupling agent to be effective for coupling and/or cross-linking polymers chains.

[0008] (b) “Phlagmatizing” refers to methods for reducing the shock sensitivity of a chemical or chemical species by mixing or combining the reactive chemical with an inert or less reactive chemical.

[0009] (c) “molecular melt” refers to an at least partially amorphous blend, at room temperature, of a coupling agent (modifying agent) and an antioxidant, optionally also containing other polymer additives. Both the coupling agent (modifying agent) and the antioxidant are at least partially contained in the amorphous phase of the blend. Also, preferably the coupling agent (modifying agent) and the antioxidant form a complex where the Raman spectra relating to the groups forming the nitrene groups are shifted compared to the Raman spectra exhibited by the groups forming the nitrene groups of the coupling agent alone.

[0010] (d) “antioxidant” refers to types or classes of chemical compounds that are capable of being used to minimize the oxidation that can occur during the processing of polymers. The term also includes chemical derivatives of the antioxidants, including hydrocarbyls. The term further includes chemical compounds, as described later in the description of the antioxidant, that when properly combined with the coupling agent (modifying agent) interact with to form a complex which exhibits a modified Raman spectra compared to the coupling agent or modifying agent alone.

[0011] (e) “modifying agent” refers to a chemical compound that contains a reactive group capable of forming a carbene or a nitrene group that can react with a polymer chain.

[0012] (f) “target polymer” refers to a polymer that is intended to be modified by the coupling or modifying agent. The target polymer can be any polymer that contains CH, CH2, or CH3 groups, aliphatic or aromatic, of a polymer chain. Preferably, the target polymer can be any polyolefin (including polyethylene) or styrenic based polymer.

[0013] (g) “DSC” refers to a differential scanning- calorimeter or differential scanning calorimetry analysis, depending on the context it is used in. DSC is a method one of ordinary skill in the art is familiar with to determine the crystallinity of a polymer.

[0014] (h) “Nitrene group” refers to a compound having a structure R-N, where N is nitrogen capable of reacting with a polymer chain by inserting into the carbon hydrogen bonds of CH, CH2, or CH3 groups, both aliphatic and/or aromatic, of a polymer chain. It is believed that the nitrogen most preferred for inserting into the carbon hydrogen bonds has two lone pairs of electrons. R may be any atom or atoms that do not adversely interfere with the nitrogen inserting into the above-described carbon hydrogen bonds.

[0015] (i) “Carbene group” refers to a compound having a structure

R—C—R′

[0016] where C is carbon capable of reacting with a polymer chain by inserting into the carbon hydrogen bonds of CH, CH2 or CH3 groups, both aliphatic and/or aromatic, of a polymer chain. It is believed that the carbon most preferred for inserting into the carbon hydrogen bonds has one lone pair of electrons. R and R′ are independently any atom or atoms that do not adversely interfere with the carbon inserting into the above-described carbon hydrogen bonds.

[0017] (j) “DPO-BSA” refers to the following compound:

[0018] 4,4′-Oxydibenzenesulfonyl azide.

SUMMARY

[0019] It has been surprisingly discovered that, an antioxidant and a coupling agent (or modifying agent) may be blended together to form a molecular melt, and that the formation of this molecular melt can phlagmatize the coupling and/or modifying agent.

[0020] In a first aspect of the invention, a molecular melt composition is disclosed comprising: (a) an antioxidant; and (b) a coupling agent.

[0021] In a second aspect of the invention, a molecular melt composition is disclosed comprising: (a) an antioxidant; and (b) a modifying agent.

[0022] In a third aspect of the invention, a method for phlagmatizing a coupling agent contained in a liquid is disclosed comprising the step of: introducing an antioxidant into the liquid. The coupling agent, which preferably is a poly(sulfonyl azide), may be dissolved or suspended in the liquid; and the antioxidant may be introduced before or after the coupling agent is produced.

[0023] In a fourth aspect of the invention, a method for phlagmatizing a modifying agent contained in a liquid is disclosed comprising the step of: introducing an antioxidant into the liquid. The modifying agent may be dissolved or suspended in the liquid. The antioxidant may be introduced before or after the coupling agent is produced.

[0024] In a fifth aspect of the invention, a method for making a molecular melt is disclosed comprising the steps of: introducing an antioxidant into a liquid containing a coupling agent and recovering the molecular melt. If it is desired to recover the molecular melt in a dry form, it can be recovered by precipitation from the liquid, or alternatively, the molecular melt may be recovered by co-crystallizing the antioxidant and the coupling agent.

[0025] In a sixth aspect of the invention, a method is disclosed for making a coupled polymer comprising the steps of mixing a molecular melt with a polymer; and reacting the molecular melt with the polymer. Preferably, the polymer is a polyolefin, more preferably a propylene based polymer and the coupling agent is preferably a poly(sulfonyl azide). The reaction typically will take place in a polymer extruder, which will both mix the molecular melt and the polymer and provide the energy necessary to cause the reaction between the molecular melt and the target polymer.

[0026] In a seventh aspect of the invention, a method is disclosed for making a modified polymer comprising the steps of mixing a molecular melt containing a modifying agent with a polymer; and reacting the molecular melt with the polymer. In some instances, the modifying agent contained in the molecular melt may be in the form of a salt and the modified polymer that results is an ionomeric polymer.

[0027] In an eighth aspect of the invention, the coupled and/or modified polymers resulting from the reaction of a coupling agent and/or a modifying agent with a target polymer are used for wire and cable applications, such as compounds for use in jacketing, insulation and moisture curable insulation applications.

[0028] Additionally, it has been surprisingly discovered that, when the coupling agent (or modifying agent) is formed into a molecular melt, the efficiency of the coupling agent for modifying the polymer may be increased. Therefore, another aspect of the invention is the use of molecular melt to provide a more- efficient method for making modified polymers and the compositions that result from such methods. Depending on the process used, the modifying agent used, the coupling agent used, and the concentrations of the coupling agents and/or modifying agents, this can provide rheology modified polymers, functionalized polymers, and/or cross-linked polymers (including, but not limited to thermosets).

[0029] It is believed that the molecular melt will greatly ease the manufacture of coupling and modifying agents to be used for polymers. It is also believed that the polymer modification processes that use such molecular melts will be far superior in efficiency and cost effectiveness than previously described processes.

BRIEF DESCRIPTION OF THE FIGURES

[0030]FIG. 1A is a depiction of the Raman Spectra obtained from DPO-BSA, Irganox 1010, a physical mixture of DPO-BSA and Irganox 1010, and a molecular melt containing DPO-BSA and Irganox 1010.

[0031]FIG. 1B is a depiction of those portions of the Raman Spectra for the DPO-BSA, the molecular melt containing DPO-BSA and Irganox 1010, and the physical mixture of DPO-BSA and Irganox 1010 that relate to the azide stretch for the DPO-BSA.

[0032]FIG. 2 is graph depicting, the decomposition peak energy per gram of DPO-BSA in several samples which contain only DPO-BSA, DPO-BSA in a physical mixture with selected antioxidants, or DPO-BSA in a molecular melt with Irganox 1010.

[0033]FIG. 3 is a graph depicting the differential scanning calorimetry analysis obtained for DPO-BSA. The DSC shows both the melting point of the DPO-BSA and the peak decomposition energy for the DPO-BSA. The data was obtained using a Thermo Analysis Instruments 2920 modulated differential scanning calorimeter using 2200 Thermo Analysis Instruments software. The samples were contained in aluminum pans that were maintained under a nitrogen atmosphere. The temperature scan rate was 10° C./minute.

[0034]FIG. 4 is a graph depicting the differential scanning calorimetry analysis obtained for molecular melt sample A. The data was obtained in two passes, a first pass from which the total crystallinity of the sample is determined and a second pass which shows the peak decomposition energy for the molecular melt. The data was obtained using a Thermo Analysis Instruments 2920 modulated differential scanning calorimeter using 2200 Thermo Analysis Instruments software. The samples were contained in aluminum pans that were maintained under a nitrogen atmosphere. The temperature scan rate was 10° C./minute.

[0035]FIG. 5 is a graph depicting the differential scanning calorimetry analysis obtained for molecular melt sample B. The data was obtained in two passes, a first pass from which the total crystallinity of the sample is determined and a second pass which shows the peak decomposition energy for the molecular melt. The data was obtained using a Thermo Analysis Instruments 2920 modulated differential scanning calorimeter using 2200 Thermo Analysis Instruments software. The samples were contained in aluminum pans that were maintained under a nitrogen atmosphere. The temperature scan rate was 10° C./minute.

[0036]FIG. 6 is a graph depicting the differential scanning calorimetry analysis obtained for molecular melt sample C. The data was obtained in a single pass using a Thermo Analysis Instruments DSC V2.6D dual-cell differential scanning calorimeter. The endotherm shown was used to determine the crystallinity, the peak decomposition energy is also, shown for the sample. The samples were contained in aluminum pans that were maintained under a nitrogen atmosphere. The temperature scan rate was 10° C./minute.

[0037]FIG. 7 is a graph depicting the differential scanning calorimetry analysis obtained for molecular melt sample D. The data was obtained in a single pass using a Thermo Analysis Instruments DSC V2.6D dual-cell differential scanning calorimeter. The endotherm shown was used to determine the crystallinity, the peak decomposition energy is also shown for the sample. The samples were contained in aluminum pans that were maintained under a nitrogen atmosphere. The temperature scan rate was 10° C./minute.

[0038]FIG. 8 is a graph depicting the differential scanning calorimetry analysis obtained for molecular melt sample E. The data was obtained in a single pass using a Thermo Analysis Instruments DSC V2.6D dual-cell differential scanning calorimeter. The, endotherm shown was used to determine the crystallinity, the peak decomposition energy is also shown for the sample. The samples were contained in aluminum pans that were maintained under a nitrogen atmosphere. The temperature scan rate was 10° C./minute.

[0039]FIG. 9 is a graph depicting the differential scanning calorimetry analysis obtained for molecular melt sample F. The data was obtained in a single pass using a Thermo-Analysis Instruments DSC V2.6D dual-cell differential scanning calorimeter. There was no discernable endotherm present from the DSC and therefore, the total crystallinity was determined to be 0%. The peak decomposition energy is shown for the sample. The samples were contained in aluminum pans that were maintained under a nitrogen atmosphere. The temperature scan rate was 10° C./minute.

[0040]FIG. 10 is a plot of the Yoshida Correlation with the experimental value for the peak decomposition energy released from molecular melt sample B plotted.

[0041]FIG. 11 is a graph depicting the differential scanning calorimetry analysis obtained for molecular melt sample G. The data was obtained in a single pass using a Thermo Analysis Instruments DSC V2.6D dual-cell differential scanning calorimeter. The endotherm shown was used to determine the crystallinity, the peak decomposition energy is also shown for the sample. The samples were contained in aluminum pans that were maintained under a nitrogen atmosphere. The temperature scan rate was 10° C./minute.

[0042]FIG. 12 is a depiction of the Raman Spectra obtained from a molecular melt containing DPO-BSA and Chimassorb 944.

[0043]FIG. 13 is a graph depicting the differential scanning calorimetry analysis obtained for molecular melt sample H. The data was obtained in a single pass using a Thermo Analysis Instruments DSC V2.6D dual-cell differential scanning calorimeter. The endotherm shown was used to determine the crystallinity, the peak decomposition energy is also shown for the sample. The samples were contained in aluminum pans that were maintained under a nitrogen atmosphere. The temperature scan rate was 10° C./minute.

[0044]FIG. 14 is a depiction of the Raman Spectra obtained from a molecular melt containing DPO-BSA and Irganox HP 136.

[0045]FIG. 15 is a graph depicting the differential scanning calorimetry analysis obtained for molecular melt sample I. The data was obtained in a single pass using a Thermo Analysis Instruments DSC V2.6D dual-cell differential scanning calorimeter. The endotherm shown was used to determine the crystallinity, the peak decomposition energy is also shown for the sample. The samples were contained in aluminum pans that were maintained under a nitrogen atmosphere. The temperature scan rate was 10° C./minute.

[0046]FIG. 16 is a depiction of the Raman Spectra obtained from a molecular melt containing DPO-BSA and Irganox I-245.

[0047]FIG. 17 is a graph depicting the differential scanning calorimetry analysis obtained for molecular melt sample J. The data was obtained in a single pass using a Thermo Analysis Instruments DSC V2.6D dual-cell differential scanning calorimeter. The endotherm shown was used to determine the crystallinity, the peak decomposition energy is also shown for the sample. The samples were contained in aluminum pans that were maintained under a nitrogen atmosphere. The temperature scan rate was 10° C./minute.

[0048]FIG. 18 is a depiction of the Raman Spectra obtained from a molecular melt containing DPO-BSA and Irganox I-1425.

[0049]FIG. 19 is a graph depicting the differential scanning calorimetry analysis obtained for molecular melt sample K. The data was obtained in a single pass using a Thermo Analysis Instruments DSC V2.6D dual-cell differential scanning calorimeter. The endotherm shown was used to determine the crystallinity, the peak decomposition energy is also shown for the sample. The samples were contained in aluminum pans that were maintained under a nitrogen atmosphere. The temperature scan rate was 10° C./minute.

[0050]FIG. 20 is a graph depicting the differential scanning calorimetry analysis obtained for molecular melt sample L. The data was obtained in a single pass using a Thermo Analysis Instruments DSC V2.6D dual-cell differential scanning calorimeter. The endotherm shown was used to determine the crystallinity, the peak decomposition energy is also shown for the sample. The samples were contained in aluminum pans that were maintained under a nitrogen atmosphere. The temperature scan rate was 10° C./minute.

[0051]FIG. 21 is a graph depicting the toughness/stiffness for nanoparticle filled propylene polymers utilizing modified polymers of the invention as compatibilizers for the nanoparticles and the polymer matrix.

DETAILED DESCRIPTION

[0052] While this invention is susceptible of embodiment in many different forms, there are shown in the Figures, and will be described in detail herein, specific embodiments of the invention. It should be understood, however, that the present disclosure is to be considered as an exemplification of the principles of the invention and is not intended to limit the invention to the specific embodiment and examples illustrated.

[0053] The majority of the following discussion will be related to a molecular melt that is a blend of a coupling agent and an antioxidant. While the molecular melt comprised of a modifying agent and an antioxidant will not be discussed to detail, one of ordinary skill in art will realize that, unless stated otherwise, the discussions and information discussed below for the molecular melt comprised of a coupling agent and an antioxidant is also applicable for the molecular melt comprised of a modifying agent and an antioxidant.

Molecular Melt

[0054] The molecular melt is at least partially amorphous, it is believed that this amorphous nature will improve the ability of the molecular melt to phlagmatize the coupling agent. It is also believed that this amorphous nature will improve the efficiency of the molecular melt in modifying a target polymer. In many instances, it is preferable that the solubility of the molecular melt in the target polymer is higher than the solubility of the coupling agent in the target polymer.

[0055] Preferably, at least a portion of the coupling agent (modifying agent) and antioxidant present in the molecular melt form a complex, which does not adversely interfere with the utilization of the coupling agent for modifying polymers, and in which the Raman spectra relating to the nitrene forming group(s) are shifted compared to the Raman spectra exhibited by the nitrene forming groups of the coupling agent alone.

[0056]FIG. 1A shows the Raman spectra for DPO-BSA alone, IRGANOX-1010 alone, DPO-BSA combined with IRGANOX-1010 in a physical mixture having a 1:1 molar ratio of DPO-BSA to IRGANOX-1010; and a molecular melt comprised of a 1:1 molar ratio of DPO-BSA to IRGANOX-1010. FIG. 1B shows in closer detail the regions of the Raman spectra (for the DPO-BSA alone, the DPO-BSA/IRGANOX-1010 physical admixture, and the DPO-BSA/IRGANOX-1010 molecular melt) that relate to the azide stretch for the DPO-BSA. As can be seen from the FIGS, the Raman spectra for the molecular melt relating to the azide stretch has been broadened and shifted as compared to the Raman spectra for the DPO-BSA alone and for the DPO-BSA/IRGANOX-1010 physical admixture. Also note that the portion of the Raman spectra near about 2700 to about 3200 cm⁻¹ for the DPO-BSA molecular melt is similar in shape and size to the same portion of the Raman spectra for the IRGANOX-1010.

[0057] The mole ratio of coupling agent to antioxidant in the molecular melt is typically from about 1:10 to about 10: 1, preferably from about 1:2 to about 8:1, more preferably from 1:1 to 4:1. It has surprisingly been found that the overall crystallinity of the molecular melt is typically related to the mole ratio of coupling agent to antioxidant. In most instances it is preferable that the ratio of coupling agent to antioxidant in the molecular melt be adjusted to provide a molecular melt having a total crystallinity of about 99 weighted average weight percent or below (as determined by DSC and calculated as set forth in Example 2), more preferably less than about 95 weighted average weight percent, further more preferably less than about 60 weighted average weight percent, most preferably less than about 40 weighted average weight percent. And, in some instances, when there is particular concern regarding the shock sensitivity of the molecular melt, it is preferable to provide a molecular melt having a crystallinity of about 20 weighted average weight percent or below, more preferably about 10 weighted average weight percent or below, further more preferably about 5 weighted average weight percent of below, most preferably about 1 weighted average weight percent or below as determined by DSC. For a molecular melt comprised of 4,4′-Oxydibenzenesulfonylazide and tetrakis [Methylene (3,5-di-t-butyl-4-hydroxyhydrocinnamate)], the molar ratio of coupling agent to antioxidant is preferably between about 1:2 and about 4:1. In some instances, low melting polymer additives such as polyethylene glycol and/or polypropylene glycol may be included in the molecular melt. It is believed that these types of compounds may reduce the crystallinity of the molecular melt and/or reduce the shock sensitivity of the molecular melt.

[0058] The molecular melt may be formed by melt blending the coupling agent and antioxidant, by co-precipitating the coupling agent and antioxidant from a common solvent, or any other method that will provide an at least partially amorphous molecular melt.

[0059] Other compounds, in addition to the coupling agent and antioxidant, may optionally be present in the molecular melt. Preferably, the additional compounds will not adversely react with either the coupling agent or the antioxidant and will not cause the crystallinity of the molecular melt to rise significantly. However, in some instances, for example, where blocking of the molecular melt is a concern, it may be desirable to add. additional compounds which will increase the resulting crystallinity of the molecular melt. As discussed earlier, low melting materials such as polyethylene glycol and polypropylene glycol may optionally be included in the molecular melt to lower the shock-sensitivity and/or crystallinity of the molecular melt. It is preferable that the molecular melt not contain any phosphate based compounds (such as phosphite based antioxidants) as it is believed that these phosphite based compounds will adversely react with the coupling agent in the molecular melt. In general the additional compounds added to the molecular melt should be polymer additives that are typically added during the polymerization process or polymer processing process.

[0060] Examples of the additional compounds that may be-present in the molecular melt include:

[0061] Internal lubricants, such as, polyethylene glycol (PEG), polypropylene glycol (PPG), calcium stearate, glycerol mono stearate (GMS);

[0062] Compatibilizing agents, such as, Titanium di(dioctylpyrophosphosate)oxyacetate, Di(dioctylpyrophosphosate) ethylene titanate, Isopropyl tricumylphenyl titanate, Tetra(2,2 diallyloxymethyl)butyl, di(ditridecyl)phosphio zirconate, Glycidoxypropyltrimethoxysilane;

[0063] Release agents, such as, Oleamide, Stearamide, Zinc stearate, Erucamide, Aminopropyltrimethoxysilane, Bis(Glycidoxypropyl)tetramethyldisiloxane, Bis (3-(triethoxysilyl)propyl)-tetrasulfide, Bis(trimethylsilyl)urea;

[0064] Plasticizers, such as, Triisooctyl trimellitate, Epoxidized soybean oil, Di(2-ethylhexyl)adipate, Acetyl triethyl citrate, Acetyl tributyl citrate, Diisocecyl adipate, Triethyl citrate, Polybutene, Oleyl palitamide, N-stearyl erucamide, Distearyl thiodipropionate;

[0065] Ultra-Violet stabilizers, such as, 2-hydroxy-4-n-octoxybenzophenone; _(—)2-hydroxy-4-methoxy-benzophenone; sodium dicyclohexyl sulfosuccinate;

[0066] Catalyst Neutralizers, such as, metal stearates (such as calcium stearate), hydro talcites, calcium lactate, and metal oxides; and combinations thereof.

[0067] Compounds containing phosphorous in the +3 oxidation state may be added to the molecular melt in limited quantities that do not adversely react with the coupling agent or modifying agent.

[0068] The molecular melt may be formed into any convenient form, solid or liquid. The molecular melt will typically be formed into particles that can be used in a process for modifying polymers, such as polyolefins. It is generally important to ensure that the coupling agents are properly dispersed in the target polymer prior to or during reaction. The applicants have discovered that in order to improve the dispersion of the coupling agent in the target polymer, the particle size can be modified according to the mole ratio of coupling agent to antioxidant in the molecular melt. The optimum particle size also depends on the equipment to be used to react the molecular melt with a target polymer. For example, for a molecular melt comprised of 4,4′-Oxydibenzenesulfonylazide (DPO-BSA) and tetrakis [Methylene (3,5-di-t-butyl-4-hydroxyhydrocinnamate)] at a molar ratio of 1:1 where a ZSK-40 co-rotating twin-screw extruder manufactured by Werner Pfleiderer Corporation is utilized, the average diameter of the particles of molecular melt is preferably about 3000 microns or less, more preferably about 2000 microns or less. For ease of processing and handling, the particles preferably have an average diameter of at least about 200 microns.

[0069] The particles may be formed using methods such as rotoforming, which provides uniformly sized and shaped particles from a flowable melt. Alternatively, methods such as prilling or spray drying or any other methods, such as milling, grinding, or tabletization may be used to generate the desired sized particles. When a highly amorphous molecular melt is desired, it is preferable to use a method that minimizes the resulting crystallinity of the molecular melt. Where blocking (or agglomeration) of the molecular melt is a concern, it is desirable to produce a molecular melt having a relatively high crystallinity. This high crystallinity will minimize or prevent the molecular melt particles from agglomerating. An example of a compound that may increase the crystallinity of the molecular melt is octacecyl-3-(3,5-di-tert.butyl-4-hydroxyphenyl)-propionate, a hindered phenol primary antioxidant available from the Ciba Specialty Chemicals Company under the trade name IRGANOX 1076 (I-1076). I-1076 can be optionally used as the second antioxidant with another more amorphous antioxidant as the first antioxidant in a molecular melt, as described in Example 14 below.

[0070] Coupling Agents and Modifying Agents:

[0071] As discussed earlier, the modifying agents and coupling agents of the invention are chemical compounds that contain at least one reactive group capable of forming a carbene or nitrene group. A modifying agent will have one such reactive group. A coupling agent will have two or more such reactive groups.

[0072] Examples of chemical compounds that contain at least one reactive group capable of forming carbene groups, include, for example, diazo alkanes, geminally-substituted methylene groups, ketenes, and metallocarbenes.

[0073] Examples of chemical compounds that contain at least one reactive group capable of forming a nitrene group, include, for example, silyl azides, phosphazene azides, sulfonyl azides, formyl azides, azides, salts of N-chlorosulfonamides, N,N-dichlorosulfonamides, and 2-trialkyl-1-sulfonylhydrazides (inner salt).

[0074] In general, the coupling agents and modifying agents have a structure RX_(n) where each X independently designates a reactive group capable of forming a carbene or nitrene group and R represents a substituted, unsubstituted or inertly substituted hydrocarbyl, hydrocarbyl ether, hydrocarbyl polyether, sulfur, or silicon-containing group. Optionally, R has more than one oxygen, sulfur, or silicon in its backbone. Silicon containing groups include silanes and siloxanes, preferably siloxanes. The term inertly substituted refers to a substitution with atoms or groups that do not undesirably interfere with the desired reaction(s) or desired properties of the resulting modified polymer.

[0075] For a modifying agent, n=1. For a modifying agent, R is preferably functionalized with a heteroatom or group. The functional group is selected from groups that do not undesirably react with the reactive group that is capable of forming the carbene and/or nitrene group. In some instances it may be necessary to protect the functional group with a protecting group that minimizes the heteroatoms interaction with the reactive group (or the azide or carbene that is formed from the reactive group). This protecting group may be removed by a subsequent reaction. In some embodiments, it is preferable for R to be large enough to increase the solubility of the modifying agent in the target polymer. In these instances, R preferably has a total of at least about 10 carbon, oxygen, sulfur, and silicon atoms, more preferably at least about 20 carbon, oxygen, sulfur, and silicon atoms. Most preferably, the modifying agent has a long aliphatic or substituted aliphatic chain of at least about 30 atoms, more preferably at least about 40 atoms. It is believed that increasing the solubility of the modifying agent, will increase the dispersion of the modifying agent within the target polymer.

[0076] Examples of functional heteroatoms or groups that may be included in a modifying

[0077] agent include, but are not limited, to the following:

[0078] Which are respectively an amino, a hydroxy, a carboxylic acid, an ester, an isocyanate, a quaternary ammonium salt, an acrylate, an amide, an anhydride, and an epoxy group. Where R″′ represents any atom or group of atoms that do not adversely interfere with a reactive carbon of a carbene group (or a reactive nitrogen of a nitrene group) inserting into the carbon hydrogen bond of a target polymer; and N represents a nitrogen, O represents an oxygen, H represents a hydrogen, C represents a carbon, and Y represents a counter anion which may or may not be present after the group is incorporated into the modifying agent. Imides, silanes, and siloxanes are other examples of groups that may be incorporated into a modifying agent.

[0079] Using modifying agents to prepare functionalized polymers is especially useful for homopolymer and copolymers of ethylene and propylene. The transition metal catalysts commonly used to prepare these polyolefins are intolerant of heteroatoms. It is possible to use radical initiators to graft functionalized unsaturated monomers to such polyolefins. However, this is difficult to accomplish without substantial loss of molecular weight, especially for polypropylene.- It is because of these synthetic difficulties that there are very few commercially available propylene based polymers with attached functional groups.

[0080] The functional groups are useful for a wide range of applications. For example, carboxylic acid functionality can be used to improve adhesion to metals, other polymers, and fillers. Polyolefins with pendant anhydride functionality are used commercially as adhesives and compatibilizers for polyolefin/Nylon blends, as well as other uses. The used of modifying agents which are ionic can have a profound influence on polymer properties. For example, ionomeric polyethylene is a very tough material with excellent melt strength in comparison to neutral polyethylene.

[0081] In addition to improving the surface characteristic of polymers, using a modifying agent according to the current invention to modify a polymer is useful for covalently binding anti-static agents, anti-microbials, antioxidants, mold-release agents, UV-stabilizers, and flame retardants. Covalently binding such functionality to the polymer eliminates the problems of bleeding and leaching of the additives.

[0082] For a coupling agent, n is greater than one. For a coupling agent, R preferably represents an unsubstituted or inertly substituted hydrocarbyl, hydrocarbyl ether or silicon-containing group. While there is no critical limit to the length of R, each R preferably had sufficient carbon, sulfur, oxygen, or silicon atoms to separate the reactive groups sufficiently to permit a facile reaction between the target polymer(s) and the sulfonyl azide, more preferably at least 1, most preferably at least 2, further more preferably at least 3 carbon, oxygen, sulfur, or silicon atoms between the reactive groups. Preferably, carbon atoms separate the reactive groups. R preferably has a total of less than about 50 carbon, sulfur, oxygen, or silicon atoms in the backbone that separates reactive groups, more preferably less than about 20, most preferably less than about 15 total carbon, sulfur, oxygen, or silicon atoms. However, in some aspects it may be preferable to use a backbone that is longer and therefore increases the solubility of the coupling agent in the target polymer. In this aspect it is preferable that the backbone contain at least about 10 total carbon, sulfur, oxygen, or silicon atoms, more preferably at least about 20 total carbon, sulfur, oxygen, or silicon atoms, most preferably at least about 30 total carbon, sulfur, oxygen, or silicon atoms. In some embodiments, it is preferable that R contain a long aliphatic or substituted aliphatic chain as a side group, preferably, the chain contains at least about 10 total carbon, sulfur, oxygen, or silicon atoms, more preferably at least about 20 total carbon, sulfur, oxygen, or silicon atoms, most preferably at least about 30 total carbon, sulfur, oxygen, or silicon atoms. It is believed that this side group will increase the dispersion of the coupling agent in the target polymer.

[0083] In order to reduce the cost of manufacturing the coupling agent, it may be advantageous for the reactive groups (X's) for a given coupling agent to be the same. In other situations, it may be desirable for a coupling agent to contain two or more different types of reactive groups (X's). For example, if two target polymers having differing melt temperatures are to be coupled, it can be desirable to use a coupling agent that contains two different reactive groups which are activated at different temperatures.

[0084] In a preferred embodiment of the invention, the target polymer is a polyolefin and the coupling agent is a poly(sulfonyl azide).. A poly(sulfonyl azide) is any compound having at least two reactive groups (the sulfonyl azide groups (—SO₂N₃)), which are reactive with the polyolefin. Preferably the poly(sulfonyl azide)s have a structure X-R-X wherein each X is SO₂N₃ and R represents an unsubstituted or inertly substituted hydrocarbyl, hydrocarbyl ether or silicon-containing group, preferably having sufficient carbon, oxygen or silicon, preferably carbon, atoms to separate the sulfonyl azide groups sufficiently to permit a facile reaction between the polyolefin and the sulfonyl azide. Examples of atoms or groups that may be inertly substituted into R include, groups such as fluorine, aliphatic or aromatic ether, siloxane as well as sulfonyl azide groups when more than two polyolefin chains are to be joined. R is suitably aryl, alkyl, aryl alkaryl, arylalkyl silane, siloxane or heterocyclic,. groups and other groups which are inert and separate the sulfonyl azide groups as described. More preferably R includes at least one aryl group between the sulfonyl groups, most preferably at least two aryl groups (such as when R is 4,4′ diphenylether or 4,4′-biphenyl). When R is one aryl group, it is preferred that the group have more than one ring, as in the case of naphthylene bis(sulfonyl azides). Poly(sulfonyl)azides include such compounds as 1,5-pentane bis(sulfonylazide), 1,8-octane bis(sulfonyl azide), 1,10-decane bis(sulfonyl azide), 1,10-octadecane bis(sulfonyl azide), 1-octyl-2,4,6-benzene tris(sulfonyl azide), 4,4′-diphenyl ether bis(sulfonyl azide), 1,6-bis(4′-sulfonazidophenyl)hexane, 2,7-naphthalene bis(sulfonyl azide), and mixed sulfonyl azides of chlorinated aliphatic hydrocarbons containing an average of from 1 to 8 chlorine atoms and from about 2 to 5 sulfonyl azide groups per molecule, and mixtures thereof. Preferred poly(sulfonyl azide)s include oxy-bis(4-sulfonylazidobenzene), 2,7-naphthalene bis(sulfonyl azido), 4,4′-bis(sulfonyl azido)biphenyl, 4,4′-diphenyl ether bis(sulfonyl azide) and bis(4-sulfonyl azidophenyl)methane, and mixtures thereof.

[0085] Sulfonyl azides are conveniently prepared by the reaction of sodium azide with the corresponding sulfonyl chloride, although nitrosation and dehydration of sulfonyl hydazines with various reagents (nitrous acid, dinitrogen tetroxide, nitrosonium tetrafluoroborate) has been used.

[0086] The following discussion regarding the coupling reaction mechanism provides the inventors current theories, but is not intended to limit the scope of the invention. Sulfonyl azides decompose in several ways, but for the practice of the invention, the reactive species is believed to be the singlet nitrene as evidenced by insertion into C—H bonds is desired. Thermal decomposition is reported to give an intermediate singlet sulfonyl nitrene, which will react readily by insertion into carbon-hydrogen bonds. The temperatures necessary for efficient formation of the sulfonyl nitrene is usually greater than about 150° C. U.S. patent application Ser. No. 09/133,576 filed Aug. 13, 1998 contains additional teachings regarding sulfonyl azides and their use for modifying polyolefins. U.S. patent application Ser. No. 09/133,576 is incorporated by reference herein in its entirety.

[0087] Where the target polymer is to be heavily cross-linked, for example when it is desirable to form a thermoset or thermoplastic vulcanate (TPV), it can be preferable to utilize a coupling agent which contains more than two reactive groups capable of forming nitrene and/or carbene groups.

[0088] Antioxidants:

[0089] The antioxidants of the invention include chemicals that are useful as antioxidants for polymers and chemical derivatives of such antioxidants, including hydrocarbyls. Preferably, the antioxidant is not a phosphite-containing compound or a compound containing a phosphorous in the +3 oxidation state, as it is believed these compounds are highly reactive with the typical coupling agents utilized in the invention. An example of a phosphite-based antioxidant is Tris(2,4-di-tert-butylphenyl)phosphite available from Ciba Specialty Chemicals Company under the trade name Irgafos 168.

[0090] The antioxidants that can be utilized in the invention also include chemical compounds that can form a complex with the coupling agent or modifying agent which does not adversely interfere with the utilization of the coupling or modifying agent for modifying polymers and where the Raman spectra relating to the groups forming the nitrene group(s) of the complex are shifted compared to the Raman spectra exhibited by the groups forming the nitrene group(s) of the coupling agent or modifying agent alone.

[0091] It is preferred, but not necessary, that the chemical compounds utilized for the antioxidant of the invention, be capable of acting as antioxidants when the molecular melt is added to the target polymer.

[0092] The antioxidants utilized preferably have the capability of existing in an amorphous state. The antioxidant is preferably more soluble in the target polymer than the coupling agent at the typically processing conditions present during the modification of the target polymer. Also, the coupling agent should be chemically and sterically compatible with the antioxidant, so as to form a partially amorphous molecular melt wherein the reactive groups of the coupling agent do not appreciably adversely react with the antioxidant.

[0093] During the manufacture of the molecular melt, it is important to minimize the chance that dry crystalline coupling agent is present in a purified form, if the coupling agent is shock sensitive.

[0094] Phlagmatization can be achieved by dilution of the coupling agent with non-shock sensitive materials. Phlagmatization is achieved when the total energy released (per weight of molecular melt) by the molecular melt in a DSC is low enough for the molecular melt to not be shock sensitive as taught by Yoshida in Kogyo Kayaku, Vol. 48 (No. 5), 1987, pp 311-316. Preferably, the total energy released in a DSC falls below the shock sensitivity line as shown in the Yoshida Correlation described in the same reference. FIG. 10 shows a plot of the Yoshida Correlation with the experimental value for the peak decomposition energy released from molecular melt sample B plotted. It can be seen from FIG. 10 that the plotted data from sample b is well below the shock sensitivity line.

[0095] The amorphous nature of the molecular melt minimizes and/or prevents the segregation of the coupling agent and antioxidant during the shipping and handling of the molecular melt.

[0096] Examples of classes of antioxidants that can be utilized in the invention include compounds which can function as either carbon radical and/or oxygen radical scavengers, such as, phenolic compounds and derivatives thereof, hindered amines, amine hydroxides, thioester compounds, and hindered phenolic compounds. Additionally, lactones, which it is believed can function as both carbon radical scavengers and oxygen radical scavengers are also included within the antioxidants which can be utilized in the invention. In some instances it may be preferable for the molecular melt to contain a mixture of antioxidants. An example of a lactone suitable for use in the invention is 5,7-bis(1,1-dimethylethyl)-3-hydroxy-2(3H)-benzofuranone reaction products with o-xylene (Chemical Abstracts # 181314-48-7), which is sold by the Ciba Specialty Chemicals Company, under the trade name IRGANOX HP-136.

[0097] The phenolic-based antioxidants and derivatives thereof and the lactones are preferred. Examples of phenolic-based antioxidants and substituted phenolic-based antioxidants include 2,2′-methylene bis(6-(1-methylcyclohexyl)-p-cresol and 2,6-ditertiary butyl-4-methyl phenol. It is believed that these classes of antioxidants are capable of forming highly amorphous (less than 10% crystallinity) molecular melts and are also capable of forming molecular melts having a high molar ratio of coupling agent to antioxidant (greater than 1:1). More preferably, the hindered phenolic compounds are utilized to form the molecular melt. An example of a hindered phenolic compound suitable for use in the invention is tetrakis [Methylene (3,5-di-t-butyl-4-hydroxyhydrocinnamate)] which is available from the Ciba Specialty Chemicals Company under the trade name Irganox 1010 (sometimes referred to as, “I-1010”).

[0098] Protection of Azide From Reaction:

[0099] The antioxidant in the molecular melt will at least partially protect the coupling agent from reacting with itself and other chemical compounds, such as compounds containing phosphorous in the +3 oxidation state that may adversely react with the coupling agent. By protecting the coupling agent, the antioxidant will increase the percentage of coupling agent that is available for reaction with the target polymer. This will increase the coupling efficiency of the coupling agent (i.e. less coupling agent wasted by side reactions

[0100] Table 1 provides the decomposition peak energy (in Joules per gram of sample (J/g) released from several samples that were obtained using a Thermo Analysis Instruments 2920 modulated differential scanning calorimeter using 2200 Thermo Analysis Instruments software. The samples were contained in aluminum pans that were maintained under a nitrogen atmosphere. The temperature scan rate was 10° C./minute. TABLE 1 Additive BSA Conc CONC Decomp Decomp Decomp Normalized (weight (weight Peak (J/g Peak (J/g Peak (J/g Average Min (J/g Max (J/g Mi- (J/g DSC Run percent) percent sample 1) sample 2) sample 3) (J/g sample) Std. Dev. sample) sample) nus Plus DPO-BSA) Irgafos 168 (physical Mixture) Baseline 0.00% 100.00% 1530.9 1,530.90 — 1,530.90 1,530.90 — — 1,530.90 2 37.03% 62.97% 511.19 511.19 — 511.19 511.19 — — 811.78 3 48.19% 51.81% 331.5 331.50 — 331.50 331.50 — — 639.87 4 67.63% 32.37% 94.1 94.10 — 94.10 94.10 — — 290.72 5 80.11% 19.89% 2.8 2.80 — 2.80 2.80 — — 14.08 Irganox 1010 (physical Mixture) Baseline 0.00% 100.00% 1530.9 1,530.90 — 1,530.90 1,530.90 — — 1,530.90 2 10.22% 89.78% 892.2 892.20 — 892.20 892.20 — — 993.72 3 34.37% 65.63% 600.7 600.70 — 600.70 600.70 — — 915.35 4 52.49% 47.51% 492 439.03 527.08 486.04 44.33 439.03 527.08 47.01 41.04 1,023.08 5 66.84% 33.16% 421.9 369.46 378.12 389.83 28.11 369.46 421.90 20.37 32.07 1,175.73 6 75.09% 24.91% 312.49 312.49 — 312.49 312.49 — — 1,254.42 7 80.15% 19.85% 195.42 264.85 303.42 254.56 54.73 195.42 303.42 59.14 48.86 1,282.39 8 91.62% 8.38% 133.34 133.34 — 133.34 133.34 — — 1,591.19 Irganox HP136 (physical Mixture) Baseline 0.00% 100.00% 1530.9 1,530.90 — 1,530.90 1,530.90 — — 1,530.90 2 34.93% 65.07% 789.6 789.60 — 789.60 789.60 — — 1,213.43 3 49.26% 50.74% 574.6 574.60 — 574.60 574.60 — — 1,132.36 4 67.04% 32.96% 419.29 419.29 — 419.29 419.29 — — 1,272.08 5 80.23% 19.77% 262.6 262.60 — 262.60 262.60 — — 1,328.22 6 88.03% 11.97% 179.85 179.85 — 179.85 179.85 — — 1,502.50 BSA/1010 (molecular Melt) Baseline 0.00% 100.00% 1530.9 1,530.90 — 1,530.90 1,530.90 — — 1,530.90 2 45.26% 54.74% 639.18 639.18 — 639.18 639.18 — — 1,167.57 3 63.01% 36.99% 471.23 471.23 — 471.23 471.23 — — 1,273.87 4 75.61% 24.39% 328.8 342.7 301.7 324.40 20.85 301.70 342.70 22.70 18.30 1,330.04 5 88.07% 11.93% 230.23 230.23 — 230.23 230.23 — — 1,929.55

[0101] All the samples were of approximately equivalent size and contained either DPO-BSA alone (the Baseline DSC runs in Table 1) or DPO-BSA with an additive. The samples used were all physical mixtures of BSA and the designated additive, wherein the dry components were physically mixed together. The final set of samples used were all molecular melts of the DPO-BSA with Irganox 1010. For some of the runs, more than one sample was analyzed and the average value obtained from the samples were recorded.

[0102] Table 1 also provides, for each sample, a value of the decomposition peak energy released from the sample normalized to the Joules released per gram of DPO-BSA present in that particular sample. This was calculated by multiplying the decomposition peak energy per gram of sample times 1/weight fraction of the DPO-BSA present in that particular sample. This provides a value for the decomposition peak energy released that is directly comparable to the decomposition peak energy released from a sample containing 100% DPO-BSA. These normalized values for the decomposition peak energy released are plotted in FIG. 2.

[0103] As can be seen from FIG. 2, the normalized decomposition peak energy released by a sample of molecular melt containing DPO-BSA and Irganox 1010 is higher than the normalized decomposition peak energy released by a sample made from a physical mixture of DPO-BSA and Irganox 1010 that contains equivalent percentages of DPO-BSA and Irganox 1010. It is believed the higher decomposition peak energies for the molecular melt indicate that the molecular melt is minimizing the self-reaction of the DPO-BSA and/or the reaction between the DPO-BSA and the Irganox 1010 as compared to the sample that is a physical mixture of DPO-BSA and Irganox 1010. When the molecular melt is used to modify a target polymer, this protective action will increase the coupling efficiency of the coupling agent for modifying the target polymer.

[0104] Additionally, the data acquired from the physical admixture of the DPO-BSA with Irgafos 168 clearly shows that the presence of a compound containing phosphorous in the +3 oxidation state reduces the decomposition peak energy released by the DPO-BSA and therefore it will reduce the coupling efficiency of the coupling agent unless other steps are taken to reduce this effect. It is believed that the addition of a coupling agent to the target polymer together with an antioxidant, even if not added as a molecular melt, will at least partially protect the coupling agent from reaction with itself and other chemicals compounds, such as compounds containing phosphorous in the +3 oxidative state.

Polymers Modified With Molecular Melt

[0105] The molecular melt can be used to modify any target polymer, preferably the target polymer is a styrenic or polyolefin (including ethylene) based polymers. Polyolefins are formed by means within the skill in the art. The alpha olefin monomers and optionally other addition polymerizable monomers are polymerized under conditions within the skill in the art, for instance as disclosed by Galli, et al., Angew. Macromol. Chem., Vol. 120, p. 73 (1984), or by E. P. More, et al. in Polypropylene Handbook, Hanser Publishers, New York, 1996, particularly pages 11 -98.

[0106] Examples of the preferred target polymers include polymers based on ethylene, propylene, and other olefins, as well as styrene, substituted styrene, and/or ethylene styrene interpolymers, as disclosed in U.S. Pat. No. 5,703,187 issued Dec. 30, 1997, whose teachings regarding ethylene styrene interpolymers and methods for making such interpolymer are incorporated by reference herein. The most preferred target polymers are polyolefin-based polymers, including propylene homopolymer, as well as random and impact copolymers of propylene and polyethylene polymers, such as high density (HDPE), medium density (MDPE), linear low density (LLDPE) and low density (LDPE) polyethylenes. Such polymers include terpolymers, tetrapolymers and higher order polymers of propylene, ethylene and other olefins, optionally, dienes and/or trienes.

[0107] Impact propylene copolymers are commercially available and are well within the skill in the art, for instance, as described by E. P. Moore, Jr in Polypropylene Handbook, Hanser Publishers, 1996, page 220-221 and U.S. Pat. Nos. 3,893,989 and 4,113,802. The term “impact copolymer” is used herein to refer to heterophasic propylene copolymers where polypropylene is the continuous phase and an elastomeric phase is uniformly dispersed therein. The impact copolymers result from an in-reactor process rather than physical blending. Usually the impact copolymers are formed in a dual or multi-stage process, which optionally involves a single reactor with at least two process stages taking place therein, or optionally multiple reactors. Advantageously, the impact copolymers have at least about 5 weight percent, preferably at least about 10, preferably up to about 40, more preferably up to about 25 weight percent, and most preferably up to about 20 weight percent polymeric units derived from ethylene. Illustrative impact copolymer propylene polymers include those available from The Dow Chemical Company under the trade designations Dow C104-01 PP, Dow C105-02 PP, Dow C 107-04 PP, and Dow DC-111 PP propylene impact copolymers having melt flow rates of 1, 2, 4, and 0.8 g/10 min, respectively, under a weight of 2.16 kg at a temperature of 230° C.

[0108] The molecular melt can be utilized to modify blends of polymers, including blends where more than one of the polymers present in the blend is capable of acting as a target polymer. It is believed the coupling agent will at least partially couple one polymer in the blend to another of the blend. Thereby, forming a compatibilizer, which will improve the compatibility of the polymers of the blend for each other.

[0109] The following discussion will specifically address the reaction of the coupling agent with polyolefins, however, one of ordinary skill in the art will realize that the teachings herein also apply to the reaction of a coupling agent and/or modifying agent with other target polymers of interest.

[0110] The reactive groups of the coupling agent are typically activated by heat, sonic energy, radiation or other chemical activating energy to generate nitrene(s) or/or carbene(s) groups which are capable of reacting with the target polymer. When the coupling agent reacts with a polyolefin, at least two separate polyolefin chains are advantageously joined and the molecular weight of the polymer chain is increased. In a preferred embodiment of the invention where the coupling agent is a bis(sulfonyl azide), two polyolefin chains are advantageously joined.

[0111] The more preferred method for activating a coupling agent is to heat the coupling agent to cause decomposition of the reactive groups to form carbene(s) and/or nitrene(s). Each coupling agent will have a characteristic temperature profile, under which it decomposes. This temperature profile can be determined by differential scanning calorimetry analysis. Each coupling agent will have a peak or a series of peak decomposition temperatures, which correspond the decomposition of a particular reactive group. For example, a differential scanning calorimeter (DSC) thermogram of the bis (sulfonyl azide) of diphenyl oxide shows a broad exothermic peak that begins about 130° C., peaks at about 185° C. (referred to herein as the peak decomposition temperature) and is complete by about 220° C. The total amount of energy released due to decomposition of the sulfonyl azide groups in the DPO-BSA is about 1500 Joules/gram.

[0112] However, most coupling agents will also decompose at temperatures less than the peak decomposition temperature. Preferably, the target polymers and the molecular melt are well mixed as the reaction between the coupling agent and the target polymer takes place. In some embodiments of the invention, it is preferable to maintain the mixture of molecular melt and target polymer well below the peak decomposition temperature until the coupling reaction is desired to take place.

[0113] Any equipment is suitably used for modifying the target polymer. Preferably, equipment which provides sufficient mixing and temperature control in the same equipment is used, but advantageously the practice of the invention takes place in such devices as an extruder, melt mixer, pump conveyor or other or a polymer mixing devise such as a Brabender melt mixer. The term extruder is used for its broadest meaning to include such devices as a device which extrudes articles, including strands or pellets. Preferably the equipment allows a sequence of temperatures or zones having different temperatures. The reaction is especially suitable for an extruder because practice of the invention can occur in a single vessel (that is any single piece of equipment capable of containing polymer). Conveniently, when there is a melt extrusion step between production of the target polymer and its use, at least one step of the process of the invention takes place in the melt extrusion step. While it is within the scope of the invention that the reaction take place in a solvent or other medium, it is preferred that the reaction be in a bulk phase to avoid later steps for removal of the solvent or other medium. For this purpose, a polymer above the softening temperature is advantageous for even mixing and for reaching a reaction temperature (which may be well below the peak decomposition temperature determined by DSC for the coupling agent).

[0114] In a preferred embodiment the process of the present invention takes place in a single vessel, that is mixing of the molecular melt and target polymer takes place in the same vessel as heating to the decomposition temperature of the coupling agent. The vessel is most preferably a twin-screw extruder, but preferably a single-screw extruder or advantageously a melt mixer, including a batch mixer. The reaction vessel more preferably has at least two zones of different temperatures into which a reaction mixture would pass, the first zone advantageously being at a temperature low enough to minimize any reaction between the coupling agent and the target polymer. In preferred practice, this first zone will mechanically mix the molecular melt and target polymer while simultaneously transporting them to a second zone. Preferably, the target polymer will not be significantly reacted in this first zone. For propylene polymers, the target polymer preferably is not significantly melted in this first zone. The second zone is preferably configured to rapidly mix the molecular melt and target polymer, while at the same time adding sufficient heat to cause the coupling agent to react with the target polymer.

[0115] Typically, an extruder is configured and operated in such a manner as to cause a temperature profile across the extruder. The term “temperature profile” is used herein to mean a series of temperatures to which the polymer is exposed. Each temperature is generally associated with a zone of the extruder. As discussed earlier, the temperature series preferably comprises a first temperature in the zone where the target polymer and molecular melt enter the extruder. In this zone the molecular melt and target polymer preferably are physically mixed, but the heat addition and temperature preferably are low enough so as not to cause or to minimize the reaction between the coupling agent and the target polymer. For a system comprised of polypropylene as the target polymer and DPO-BSA as the coupling agent, it has been found that this first temperature should preferably be at or below about 170° C., more preferably at or below about 140° C., most preferably at or below about 130° C., and in some instances at or below about 120° C.

[0116] The temperature profile also preferably comprises a second temperature which is typically associated with the second zone of the extruder. In the second zone enough heat is added to cause significant reaction between the coupling agent and the target polymer. This second zone is preferably at a temperature of at least the peak decomposition temperature of the coupling agent. The second zone is preferably followed by one, more preferably four, most preferably at least five additional zones where the polymer is mixed and the temperature is controlled. Within the second and following zones, there preferably is at least one temperature which is at least 5, most preferably at least 20, even more preferably at least 35° C. above the peak decomposition temperature of the coupling agent. For a system comprised of polypropylene as the target polymer and DPO-BSA as the coupling agent, stream temperatures of greater than 250° C. are preferably avoided while there is significant unreacted DPO-BSA in the reaction mixture.

[0117] In the description of the temperature profile of the extruder for the invention, unless otherwise stated, the temperatures are the stream temperatures, that is temperatures inside the polymer stream or polymer melt rather than the temperatures of the equipment which are understood by those skilled in the art to be likely to be lower or higher than stream temperatures because of imperfect heat transfer into the polymer or induced shear heating of the polymer. Those skilled in the art can determine the relationship between stream temperature and equipment or gage temperature of particular equipment without undue experimentation. It is known in the art that the polymer stream temperature is advantageously close to the machine set temperature in the initial zones of an extruder, but the polymer stream temperature can often be greater than the machine set temperatures in the latter zones of the extruder as it approaches the exit die of the extruder due to mechanically induced shear heating.

[0118] Coupling Agent for Rheological Modification:

[0119] Those skilled in the art will recognize that the reactivity of the coupling agent, the coupling agent and the desired or predetermined rheology or amount of chain coupling determine the amount of coupling agent to be used. Determining this amount is within the skill in the art. In this aspect of the invention, formation of substantially crosslinked networks is to be avoided because the resulting material would be intractable; therefore, poly(sulfonyl azide) is preferably limited to that amount which results in chain coupled or rheology modified, (but not substantially crosslinked) polyolefin. However, some applications will tolerate a certain amount of crosslinking (such as foam applications). In general the level of azide used preferably is less than about 1.6 mole coupling agent per mole of target polymer. For films preferably less than about 0.5 weight percent, more preferably less than about 0.20 weight percent, most preferably less than about 0.10 weight percent of the preferred coupling agent poly(sulfonyl azide) based on the total weight of polyolefin, preferably polypropylene or polypropylene/ethylene copolymer blend.

[0120] Crosslinking is evidenced by gel formation which is measured in the case of polypropylene by measuring the amount of gels in a cast film, either by eye or camera.

[0121] When poly(sulfonyl azide) is used in the practice of the invention, at least about 0.005 weight percent poly(sulfonyl azide) is advantageously used to achieve measurable results, preferably at least about 0.01 weight percent, more preferably at least about 0.02 weight percent. In some instances, it is preferable to use at least about 0.05 weight percent poly(sulfonyl azide) based on total weight of polymer(s).

[0122] Coupling Agent for Cross-linking:

[0123] As with rheology modification, those skilled in the art will recognize that the reactivity, the coupling agent used and desired degree of cross-linking will determine the amount of coupling agent used. However, unlike rheology modification, for cross-linking applications, it is necessary to add sufficient coupling agent to form cross-linked networks. This requires a higher concentration of reactive groups capable of forming carbene or nitrene groups be used for each polymer molecule. Typically, the molar ratio of reactive groups to target polymers should be from about 0.9 to about 6.0. In some embodiments, it is preferred to use coupling agents having greater than two reactive groups per coupling agent molecule. This will reduce the amount of coupling agent that must be used. Also, for cross-linked applications, it is typically desirable to minimize the amount of antioxidant added to the target polymer. Therefore, it is preferable in these applications that the molecular melt utilized have a relatively higher molar ratio of coupling agent to antioxidant than the molecular melt typically utilized for rheology modification.

EXAMPLES Example 1 4,4′-Oxydibenzenesulfonyl Azide (DPO-BSA) Manufacturing Process

[0124] DPO-BSA is manufactured in a batch process using a glass lined stirred reactor which is equipped with a jacket for cooling/heating, bottom drain valve, condenser, thermowell, and a nitrogen pad. Toluene from recycle (186.83 g) (recovered from washing the DPO-BSA product crystals) and recovered toluene from the compounding process (66.9 g) is charged to the reactor. This is heated to 50° C. and 96.1 g of 4,4′-oxydibenzenesulfonyl chloride (DPO-BSC) is added while stirring. To the reactor 87.78 g of recycle water from the water wash of the previous reaction is than added and the stirrer set at 150 rpm. 0.24 g of NaHCO3 is then added to neutralize any acid in the solution. When a pH paper confirms that the water phase is neutral then 0.24 g of tetra-n-butyl-ammonium chloride (PTC) is added. To this is added 35 g of sodium azide over fifteen minutes. The stirrer rpm can be increased to 300 to insure proper mixing of the phases. The reactor temperature is increased from 50° C. to 65° C. over 30 minutes. The reaction is 100% converted in 75 minutes as confirmed by Liquid Chromatography analysis. The stirrer is turned off and the phases allowed to separate for 10 minutes. The bottom water/salt phase is removed using the bottom drain valve and sent to the on site incinerator. An additional 29.33 g of 55° C. water is added and the stirrer set at 250 rpm for 5 minutes then turned off and the phases allowed to separate (10 minutes). The bottom phase is again removed and the water extraction step is repeated two more times (2×29.33 g of 55° C. water). The stirrer rpm is reduced to 200 for the subsequent extractions to insure that a permanent emulsion does not occur. All three washes are combined and held for recycle to the next batch. When the water phases have been removed the temperature is cooled to 10° C. and held there for 60 minutes before the bottom valve is opened and the precipitated DPO-BSA slurry transferred into a filter where it is collected and dried to a 40% toluene wet cake under nitrogen. Approximately 101.4 g of DPO-BSA is recovered with the remaining 5.60 g staying in the toluene filtrate. This toluene filtrate is recycled into the next reaction. The 40% toluene wet cake is used directly in the compounding process. FIG. 3 is a DSC of DPO-BSA.

Example 2 4,4′-Oxydibenzenesulfonyl Azide (DPO-BSA) Melt Blend Compounding Process to Manufacture DPO-BSA:I-1010 in a 1:3.3 Weight Ratio (1.0:1.066 Molar Ratio) Molecular Melt (Molecular Melt Sample A)

[0125] DPO-BSA, obtained from example 1, is compounded in a batch process using a glass lined stirred reactor which is equipped with a jacket for cooling/heating, bottom drain valve, condenser, thermowell, and a nitrogen sparge. 4,4′-Oxydibenzenesulfonyl Azide (DPO-BSA) (101.4 g) as a wet cake (total weight of wet cake is 168.2 g, contains 40% toluene) is charged to the reactor, stirring commenced and the temperature is raised to 88° C. resulting in a clear solution. IRGANOX® 1010 (1-1010) (334.6 g) is added into mixture and stirred till a clear solution results at 94° C. The reactor is sealed and evacuated as the temperature is raised to 97° C. while toluene (66.7 g) is collected from the overhead (2 hours) and is recovered for recycle to the DPO-BSA manufacturing process. A subsurface nitrogen sparge is used in the final hour to aid in removing the toluene. When the batch is dry, the compounded polymer additive formulation is kept at 97° C. and dripped dropwise into 3000 g rapidly stirred water, cooled to 25° C., and filtered on coarse frit. The product is then washed using 500 ml water, and dried in a rotary drier at 40° C./10 mm Hg. The product is a free flowing powder which is not shock sensitive and can be handled with no special precautions. Analysis by high pressure liquid chromatography (HPLC) shows the composition of this molecular melt to be 23.7 wt. % DPO-BSA and 76.3 wt. % IRGANOX® I-1010. Differential scanning calorimetry analysis determined that the DPO-BSA:Irganox-1010 molecular melt formed by this procedure exhibited a total crystallinity of 0.42 weighted average weight percent. The weighted average weight percent is calculated by dividing the integrated melt endotherm (in J/g) by the sum of the products of the melt endotherms of the neat components multiplied by their individual weight percentages of the total molecular melt. FIG. 4 shows the differential scanning calorimetry results for Molecular Melt Sample A.

Example 3 DPO-BSA Co-precipitation Process to Manufacture DPO-BSA:I-1010 in a 1:3.3 Weight Ratio (1.0:1.066 Molar Ratio) Molecular Melt (Molecular Melt Sample B)

[0126] DPO-BSA, obtained as in Example 1, is compounded in a batch process using a glass lined stirred reactor which is equipped with a jacket for cooling/heating, bottom drain valve, condenser, thermowell, and a nitrogen sparge. 4,4′-Oxydibenzenesulfonyl Azide (DPO-BSA) (25.6 g) is charged to the reactor followed by 100 g of acetonitrile, stirring commenced and the temperature is raised to 60° C. resulting in a clear solution. IRGANOX® I-1010 (84.37 g) is added into the mixture and stirred till a clear solution results at 60° C. The reactor is sealed and evacuated as the temperature is maintained at 67° C. while acetonitrile (90 g) is collected from the overhead (2 hours) and is recovered for recycle. A subsurface nitrogen sparge is used in the final hour to aid in removing the acetonitrile. At this time, the molten compounded polymer additive formulation is kept at 57° C. and dripped dropwise into 3000 g rapidly stirred water, cooled to 25° C., and filtered on coarse frit. The product was then washed using 500 ml water, and dried in a rotary drier at 40° C./ 10 mm Hg. The product is a free flowing powder which is not shock sensitive and can be handled with no special precautions. Analysis by HPLC shows the composition of this molecular melt to be 23.7 wt. % DPO-BSA and 76.3 wt. % IRGANOX® I-1010. Differential scanning calorimetry analysis determined that the DPO-BSA:Irganox-1010 molecular melt formed by this procedure exhibited a total crystallinity of 43.7 weighted average weight percent. FIG. 5 shows the differential scanning calorimetry results for Molecular Melt Sample B.

Example 4 4,4′-Oxydibenzenesulfonyl Azide (DPO-BSA) Melt Blend Compounding Process to Manufacture DPO-BSA:I-1010 in a 1:1.7 Weight Ratio (1.82:1 Molar Ratio) Molecular Melt (Molecular Melt Sample C)

[0127] DPO-BSA, obtained as in example 1, is compounded in a batch process using a glass lined stirred reactor which is equipped with a jacket for cooling/heating, bottom drain valve, condenser, thermowell, and a nitrogen sparge. Methylene chloride (3664 g) is charged to the reactor followed by 4,4′-Oxydibenzenesulfonyl Azide (DPO-BSA) (567.84 g) and IRGANOX® I-1010 (965.32 g), stirring commenced and the temperature is raised to 88° C. resulting in a clear solution. Methylene chloride is taken overhead from the mixture till a clear melt-results at 94° C. The reactor is sealed and evacuated as the temperature is raised to 97° C. while methylene chloride (3600 g) is collected from the overhead (1.5 hours) and is recovered for recycle to the DPO-BSA compounding process. A subsurface nitrogen sparge is used in the final hour to aid in removing the methylene chloride. When the batch is dry, the compounded polymer additive formulation is kept at 97° C. and poured into a pan (32×18×4 inches), cooled to 25° C., and ground in a Franklin Miller grinder to obtain particles in the range of 200 to 2000 microns. The product was then dried in a rotary drier at 40° C./ 10 mm Hg. The product is a free flowing powder which is not shock sensitive and can be handled with no special precautions. Analysis by HPLC shows the composition of this molecular melt to be 37.04 wt. % DPO-BSA and 62.96 wt. % IRGANOX® 1-1010. Differential scanning calorimetry analysis determined that the DPO-BSA: Irganox-1010 molecular melt formed by this procedure exhibited a total crystallinity of 48.15 weighted average weight percent. FIG. 6 shows the differential scanning calorimetry results for Molecular Melt Sample C.

Example 5 4,4′-Oxydibenzenesulfonyl Azide (DPO-BSA) Melt Blend Compounding Process to Manufacture DPO-BSA:I-1010 in a 1:0.825 Weight Ratio (3.75:1 Molar Ratio) Molecular Melt (Molecular Melt Sample D)

[0128] DPO-BSA, obtained as in example 1, is compounded in a batch process using a glass lined stirred reactor which is equipped with a jacket for cooling/heating, bottom drain valve, condenser, thermowell, and a nitrogen sparge. Methylene chloride (4130 g) is charged to the reactor followed by 4,4′-Oxydibetizenesulfonyl Azide (DPO-BSA) (640.14 g) and IRGANOX® I-1010 (528.10 g), stirring commenced and the temperature is raised to 88° C. resulting in a clear solution. Methylene chloride is taken overhead from the mixture till a clear melt results at 94° C. The reactor is sealed and evacuated as the temperature is raised to 97° C. while methylene chloride (4022 g) is collected from the overhead (1.5 hours) and is recovered for recycle to the DPO-BSA compounding process. A subsurface nitrogen sparge is used in the final hour to aid in removing the methylene chloride. When the batch is dry, the compounded polymer additive formulation is kept at 97° C. and poured into a pan(32×18×4 inches), cooled to 25° C., and ground in a Franklin Miller grinder to obtain particles in the range of 200 to 2000 microns. The product was then dried in a rotary drier at 40° C./10 mm Hg. The product is a free flowing powder which is not shock sensitive and can be handled with no special precautions. Analysis by HPLC shows the composition of this molecular melt to be 54.79 wt. % DPO-BSA and 45.21 wt. % IRGANOX® I-1010. Differential scanning calorimetry analysis determined that the DPO-BSA: Irganox-1010 molecular melt formed by this procedure exhibited a total crystallinity of 51.09 weighted average weight percent. FIG. 7 shows the differential scanning calorimetry results for Molecular Melt Sample D.

Example 6 4,4′-Oxydibenzenesulfonyl Azide (DPO-BSA) Melt Blend Compounding Process to Manufacture DPO-BSA:I-1010 in a 1:6.6 Weight Ratio (1:2.13 Molar Ratio) Molecular Melt Molecular Melt Sample E)

[0129] DPO-BSA, obtained as in example 1, is compounded in a batch process using a glass lined stirred reactor which is equipped with a jacket for cooling/heating, bottom drain valve, condenser, thermowell, and a nitrogen sparge. Methylene chloride (2580 g) is charged to the reactor followed by 4,4′-Oxydibenzenesulfonyl Azide (DPO-BSA) (400.00 g) and IRGANOX® I-1010 (2640.00 g), stirring commenced and the temperature is raised to 88° C. resulting in a clear solution. Methylene chloride is taken overhead from the mixture till a clear melt results at 94° C. The reactor is sealed and evacuated as the temperature is raised to 97° C. while methylene chloride (2376 g) is collected from the overhead (1.5 hours) and is recovered for recycle to the DPO-BSA compounding process. A subsurface nitrogen sparge is used in the final hour to aid in removing the methylene chloride. When the batch is dry, the compounded polymer additive formulation is kept at 97° C. and poured into a pan (32×18×4 inches), cooled to 25° C., and ground in a Franklin Miller grinder to obtain particles in the range of 200 to 2000 microns. The product was then dried in a rotary drier at 40° C./10 mm Hg. The product is a free flowing powder which is not shock sensitive and can be handled with no special precautions. Analysis by HPLC shows the composition of this molecular melt to be 13.16 wt. % DPO-BSA and 86.84 wt. % IRGANOX® I-1010. Differential scanning calorimetry analysis determined that the DPO-BSA:Irganox-1010 molecular melt formed by this procedure exhibited a total crystallinity of 0.82 weighted average weight percent. FIG. 8 shows the differential scanning calorimetry results for Molecular Melt Sample E.

Example 7 4,4′-Oxydibenzenesulfonyl Azide (DPO-BSA) Melt Blend Compounding Process to Manufacture DPO-BSA:I-1010 in a 1:3.3 Weight Ratio (1:1.066 Molar Ratio) Molecular Melt, Large Scale Example (Molecular Melt Sample F)

[0130] DPO-BSA, obtained as in example 1, is compounded in a batch process using a glass lined stirred reactor which is equipped with a jacket for cooling/heating, bottom drain valve, condenser, thermowell, and a nitrogen sparge. Methylene chloride (129.42 kg) is charged to the reactor followed by 4,4′-Oxydibenzenesulfonyl Azide (DPO-BSA) (20.06 kg) and IRGANOX® I-1010 (66.20 kg), stirring commenced and the temperature is raised to 38° C. resulting in a clear solution. Methylene chloride is taken overhead from the mixture till a clear melt results at 94° C. The reactor is sealed and evacuated as the temperature is raised to 97° C. while methylene chloride (128.2 kg) is collected from the overhead (1.5 hours) and is recovered for recycle to the DPO-BSA compounding process. A subsurface nitrogen sparge is used in the final hour to aid in removing the methylene chloride. When the batch is dry, the compounded polymer additive formulation is kept at 97° C. and poured into 10 pans (32×18×4 inches), cooled to 25° C., and ground in a Franklin Miller grinder to obtain particles in the range of 200 to 2000 microns. The product was then dried in a rotary drier at 40° C./10 mm Hg. The product is a free flowing powder which is not shock sensitive and can be handled with no special precautions. Analysis by HPLC shows the composition of this molecular melt to be 23.26 wt. % DPO-BSA and 76.74 wt. % IRGANOX I-1010. Differential scanning calorimetry analysis determined that the DPO-BSA:Irganox-1010 molecular melt formed by this procedure exhibited a total crystallinity of 0.00 weighted average weight percent. FIG. 9 shows the differential scanning calorimetry results for Molecular Melt Sample F.

[0131] The following examples-describe additional compounds that can function as the antioxidant portion of molecular melt compositions.

Example 8 4,4′-Oxydibenzenesulfonyl Azide (DPO-BSA) Melt Blend Compounding Process to Manufacture DPO-BSA: Chimassorb 944 in a 1:6.575 Weight Ratio (1:1 Molar Ratio) Molecular Melt (Molecular Melt Sample G)

[0132] The following example demonstrates that chemical compounds that may not typically be referred to as antioxidants, but are considered as antioxidants for use in the molecular melt.

[0133] DPO-BSA, obtained as in example 1, is compounded in a batch process using a glass lined stirred reactor which is equipped with a jacket for cooling/heating, bottom drain valve, condenser, thermowell, and a nitrogen sparge. Toluene (20.00 g) is charged to the reactor followed by 4,4′-Oxydibenezenesulfonyl Azide (DPO-BSA) (2.00 g) and (Poly-[[6-(1,1,3,3-tetramethylbutyl)amino]-s-triazine-2,4-diyl][2,2,6,6-tetramethyl-4-piperidyl)imino])(13.15 g) (a hindered amine light stabilizer available from the Ciba Specialty Chemicals Company under the trade name Chimassorb® 944), stirring commenced and the temperature is raised to 80° C. resulting in a clear solution. Toluene is taken overhead under vacuum, from the mixture till a clear melt results at 85° C. When the batch is dry, the compounded polymer additive formulation is kept at 85° C. and poured into a watch glass, cooled to 25° C. The product was then dried in a vacuum oven at 40° C./1.0 mm Hg. The product is a free flowing powder which is not shock sensitive and can be handled with no special precautions. Analysis by HPLC shows the composition of this molecular melt to be 13.16 wt. % DPO-BSA and 86.84 wt. % Chimassorb® 944. Differential scanning calorimetry analysis determined that the DPO-BSA: Chimassorb® 944 molecular melt formed by this procedure exhibited a total crystallinity of 13.3% weighted average weight percent. FIG. 11 shows the differential scanning calorimetry results for Molecular Melt Sample G.

[0134] As can be seen from the Raman spectra of FIG. 12, the molecular melt composition of Sample G exhibits a doublet at approximately 2100. The left peak of the doublet is due to the DPO-BSA, the right peak of the doublet is due to the interaction of the DPO-BSA with the Chimassorb 944.

Example 9 4,4′-Oxydibenzenesulfonyl Azide (DPO-BSA) Melt Blend Compounding Process to manufacture DPO-BSA: Lactone (HP 136) in a 1:0.925 Weight Ratio (1:1 Molar Ratio) Molecular Melt (Molecular Melt Sample H)

[0135] DPO-BSA, obtained as in example 1, is compounded in a batch process using a glass lined stirred reactor which is equipped with a jacket for cooling/heating, bottom drain valve, condenser, thermowell, and a nitrogen sparge. Toluene (20.00 g) is charged to the reactor followed by 4,4′-Oxydibenezenesulfonyl Azide (DPO-BSA) (2.00 g) and (5,7-bis(1,1-dimethylethyl)-3-hydroxy-2(3H)-benzofuranone reaction products with o-xylene)(1.85 g) (a lactone based antioxidant available from the Ciba Specialty Chemicals Company under the trade name IRGANOX HP 136®), stirring commenced and the temperature is raised to 80° C. resulting in a clear solution. Toluene is taken overhead under vacuum, from the mixture till a clear melt results at 85° C. When the batch is dry, the compounded polymer additive formulation is kept at 85° C. and poured into a 100 ml bottle, cooled to 25° C. The product was then dried in a vacuum oven at 40° C./1.0 mm Hg. The product is a free flowing powder which is not shock sensitive and can be handled with no special precautions. Analysis by HPLC shows the composition of this molecular melt to be 52.0 wt. % DPO-BSA and 48.0 wt. % HP 136®. Differential scanning calorimetry analysis determined that the DPO-BSA: HP 136® molecular melt formed by this procedure exhibited a total crystallinity of 0.0% weighted average weight percent. FIG. 13 shows the differential scanning calorimetry results for Molecular Melt Sample H.

[0136] As can be seen from the Raman spectra of FIG. 14, the molecular melt composition of Sample H exhibits a doublet at approximately 2100 cm⁻¹. The left peak of the doublet is due to the DPO-BSA, the right peak of the doublet is due to the interaction of the DPO-BSA with the HP 136.

Example 10 4,4′-Oxydibenzenesulfonyl Azide (DPO-BSA) Melt Blend Compounding Process to Manufacture DPO-BSA: I-245 in a 1:1.543 Weight Ratio (1:1 Molar Ratio) Molecular Melt (Molecular Melt Sample I)

[0137] DPO-BSA, obtained as in example 1, is compounded in a batch process using a glass lined stirred reactor which is equipped with a jacket for cooling/heating, bottom drain valve, condenser, thermowell, and a nitrogen sparge. Toluene (20.00 g) is charged to the reactor followed by 4,4′-Oxydibenezenesulfonyl Azide (DPO-BSA) (3.00 g) and (ethylenebis(oxyethylene)bis-(3-(5-tert-butyl-4-hydroxy-m-tolyl)-propionate))(1.85 g) (an antioxidant available from the Ciba Specialty Chemicals Company under the trade name IRGANOX® I-245), stirring commenced and the temperature is raised to 80° C. resulting in a clear solution. Toluene is taken overhead under vacuum, from the mixture till a clear melt results at 85° C. When the batch is dry, the compounded polymer additive formulation is kept at 85° C. and poured into a 100 ml bottle, cooled to 25° C. The product was then dried in a vacuum oven at 40° C./1.0 mm Hg. The product is a free flowing powder which is not shock sensitive and can be handled with no special precautions. Analysis by HPLC shows the composition of this molecular melt to be 39.3 wt. % DPO-BSA and 60.6 wt. % IRGANOX® I-245. Differential scanning calorimetry analysis determined that the DPO-BSA: I-245 molecular melt formed by this procedure exhibited a total crystallinity of 0.0% weighted average weight percent. FIG. 15 shows the differential scanning calorimetry results for Molecular Melt Sample I.

[0138] As can be seen from the Raman spectra of FIG. 16, the molecular melt composition of Sample I exhibits a doublet at approximately 2100 cm⁻¹. The left peak of the doublet is due to the DPO-BSA, the right peak of the doublet is due to the interaction of the DPO-BSA with the Irganox I-245.

Example 11 4,4′-Oxydibenzenesulfonyl Azide (DPO-BSA) Melt Blend Compounding Process to Manufacture DPO-BSA: I-1425 in a 1:0.55 Weight Ratio (1:1 Molar Ratio) Molecular Melt (Molecular Melt Sample J)

[0139] DPO-BSA, obtained as in example 1, is compounded in a batch process using a glass lined stirred reactor which is equipped with a jacket for cooling/heating, bottom drain valve, condenser, thermowell, and a nitrogen sparge. Toluene (20.00 g) is charged to the reactor followed by 4,4′-Oxydibenezencsulfonyl Azide (DPO-BSA) (3.00 g) and (calciumdiethyl bis(((3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl)methyl) phosphonate) (5.48 g) (an antioxidant available from the Ciba Specialty Chemicals Company under the trade name IRGANOX® I-1425), stirring commenced and the temperature is raised to 80° C. resulting in a clear solution. Toluene is taken overhead under vacuum, from the mixture till a clear melt results at 85° C. When the batch is dry, the compounded polymer additive formulation is kept at 85° C. and poured into a 100 ml bottle, cooled to 25° C. The product was then dried in a vacuum oven at 40° C./1.0 mm Hg. The product is a free flowing powder which is not shock sensitive and can be handled with no special precautions. Analysis by HPLC shows the composition of this molecular melt to be 35.37 wt. % DPO-BSA and 64.63 wt. % IRGANOX® I-1425. Differential scanning calorimetry analysis determined that the DPO-BSA: I-1425 molecular melt formed by this procedure exhibited a total crystallinity of 68.76% weighted average weight percent. FIG. 17 shows the differential scanning calorimetry results for Molecular Melt Sample J.

[0140] As can be seen from the Raman spectra of FIG. 18, the molecular melt-composition of Sample J exhibits a doublet at approximately 2100 cm⁻¹. The left peak of the doublet is due to the DPO-BSA, the right peak of the doublet is due to the interaction of the DPO-BSA with the Irganox I-1425.

Example 12 4,4′-Oxydibenzenesulfonyl Azide (DPO-BSA) Melt Blend Compounding Process to Manufacture DPO-BSA:I-1010 in a 1:3.3 Weight Ratio (1:1.066 Molar Ratio) Molecular Melt (Molecular Melt Sample K)

[0141] Following is a method that can be utilized to produce a molecular melt having a higher percentage of crystallinity than the molecular melt obtained in the previous examples. The example also demonstrates that the DPO-BSA is never isolated in purified form, the I-1010 is added to the DPO-BSA while it is suspended in the toluene, to phlagmatize the DPO-BSA so that it may easily and safely be recovered from the toluene.

[0142] DPO-BSA is manufactured in a batch process using a glass lined stirred reactor which is equipped with a jacket for cooling/heating, bottom drain valve, condenser, thermowell, and a nitrogen pad. Toluene from recycle (186.83 kg) and fresh toluene (66.9. kg) is charged to the reactor. This is heated to 50° C. and 96.1 kg of 4,4′-oxydibenzenesulfonyl chloride (DPO-BSC) is added while stirring. To the reactor 87.78 kg of recycle water from the water wash of the previous reaction is than added and the stirrer set at 150 rpm. 0.24 kg of NaHCO3 is then added to neutralize any acid in the solution. When a pH paper confirms that the water phase is neutral then 0.24 kg of tetra-n-butyl-ammonium chloride (PTC) is added. To this is added 35 kg of sodium azide over fifteen minutes. The stirrer rpm is increased to 300 to insure proper mixing of the phases. The reactor temperature is increased from 50° C. to 65° C. over 30 minutes. The reaction is: 100% converted in 75 minutes as confirmed by Liquid Chromatography analysis. The stirrer is turned off and the phases allowed to separate for 10 minutes. The bottom water/salt phase is removed using the bottom drain valve and sent to the on site incinerator. An additional 29.33 kg of 55° C. water is added and the stirrer set at 250 rpm for 5 minutes then turned off and the phases allowed to separate (10 minutes). The bottom phase is again removed and the water extraction step is repeated two more times (2×29.33 kg of 55° C. water). The stirrer rpm is reduced to 200 for the subsequent extractions to insure that a permanent emulsion does not occur. All three washes are combined and held for recycle to the next batch.

[0143] IRGANOX® I-1010 (334.6 kg) is added into mixture and stirred till a clear solution results at 94° C. The reactor temperature is raised to 97° C. while toluene (186.83 kg) is collected from the overhead (2 hours) and is recovered for recycle to the DPO-BSA manufacturing process. Methanol (600 kg) is added and the remaining toluene removed via azeotropic distillation with the methanol. When the batch is free of toluene, the formulation is cooled to 5° C. and crystals are allowed to form which are then collected by centrifugation. The product is then dried in a rotary drier at 40° C./10 mm Hg. The product is a free flowing powder that is not shock sensitive and can be handled with no special precautions. Analysis by HPLC shows the composition of this molecular melt to be 23.26 wt. % DPO-BSA and 76.74 wt. % IRGANOX® I-1010. Differential scanning calorimetry analysis determined that the DPO-BSA:Irganox-1010 molecular melt formed by this procedure exhibited a total crystallinity of 76.87% weighted average weight percent. FIG. 19 shows the differential scanning calorimetry results for this Molecular Melt.

Example 13 Production of Rheology Modified Polymers using a DPO-BSA:I-1010 in a 1:3.3 Weight Ratio (1:1.066 Molar Ratio) Molecular Melt

[0144] Base Polypropylene Resin

[0145] The base polypropylene used to make the samples used in all the following examples is isotactic polypropylene pellets, available from The Dow Chemical Company under the designation Dow H700-12 PP and Dow C105-02 PP. Dow H700-12 PP is a homopolymer of propylene, melt flow rate (MFR)=12 dg/min at 230° C./2.16 kg. Dow C105-02 PP is an impact copolymer of propylene with 16-22 weight percent of ethylene, melt flow rate (MFR)=1.7 dg/min at 230° C./2.16 kg.

[0146] Preparation of Modified Polypropylenes

[0147] Polymer Samples A1, B1, and CA are produced as follows. 1500 grams of polymer were weighed into a container. 1.5 grams of oil was added and the container was then tumbled for 30 minutes. At that time, the desired amounts of Molecular Melt (1:3.3 wt ratio DPO-BSA:Irganox 1010) and additives (see Table 2) were added and the container was tumbled for an additional 30 minutes. The tumbled mixture was fed directly to a 20 mm extruder using a single vibratory feeder. The feed rate was adjusted such that 80% torque was achieved.

[0148] Polymer Samples A2, B2 and CB are produced using a powder masterbatch method as follows. Two feeders were employed, one for delivery of a powder masterbatch to deliver the additives to the extruder and the second for delivery of the base polymer. The feeders were adjusted to feed in at weight ratio of 95 to 5 base polymer to powder masterbatch. The base polymer was placed in a vibratory feeder and fed directly to the extruder. The powder masterbatch was made by weighing 100 grams of an isotactic homopolymer polypropylene powder, (Profax 6301 for example A2 and Profax 6501 for examples B2 and CB, available from Bassel), into a container. The desired amounts Molecular Melt (1:3.3 wt. ratio DPO-BSA:Irganox 1010) and additives (see Table 2) were added, such that the final concentration in the product would be achieved, and the container was tumbled for 30 minutes. The base polymer and powder masterbatch feeder were adjusted to feed to the extruder at a weight ratio of 95 to 5 base polymer to powder masterbatch and to achieve 80% torque.

[0149] The extruder used in all cases was a 20 mm Welding Engineers twin-screw extruder. The extruder was run at 200 rpm. The temperature profile across the twin screw extruder from inlet to outlet 170, 180, 190, 200, 210, 220 and 230. The temperatures listed are barrel temperatures in the extruder. A die located at the outlet of the last zone had a temperature of 240° C. to ensure the full reaction of the BSA and propylene polymer. The resulting melt-extruded polymer went though the die and was then pelletized.

[0150] Referring to Table 2, the melt flow rates (MFR) of the resulting modified polymers (Polymer Samples A1, A2, B1, and B2), measured according to ASTM method D 1238 at 230° C. with a 2.16 kg weight, are reduced compared to the unmodified polymer samples. This indicates that the polymer samples were successfully rheology modified by the reaction of DPO-BSA with the base polypropylene polymer. It is believed that the Molecular Melt will more efficiently couple the base polymer than an equivalent amount of BSA alone. TABLE 2 1:3.3 wt ratio DPO-BSA: Bisazide Irganox Iganox 1010 from 1010 from Molecular Molecular Molecular Irganox Irgafos Irganox Silicone Polymer Base Method of Melt Melt** Melt** 1010 168 B225 oil Profax Profax Sample Polymer Addition MFR (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) 6301 6501 A1 H700-12 Tumbled 3.6 2150 500 1650  0  250 0 1000 0 0 A2 H700-12 Powder 3.6 2150 500 1650  0  250 0  0 5 wt % 0 Masterbatch CA H700-12 Tumbled 12.1    0  0  0   0 500  1000 0 0 B1 C105-02 Tumbled 1.3  860 200  660 340 1000 0 1000 0 0 B2 C105-02 Powder 1.7  860 200  660 340 1000 0   0 0 5 wt % Masterbatch CB C105-02 Powder 2.0   0  0   0 1000  1000 0   0 0 5 wt % Masterbatch

Example 14 4,4′-Oxydibenzenesulfonyl Azide (DPO-BSA) Melt Blend Compounding Process to Manufacture DPO-BSA:I-1010:I-1076 in a 1:3.3:1.4 weight ratio (1:1:1 molar ratio) molecular melt (Molecular Melt Sample L)

[0151] DPO-BSA, obtained as in example 1, is compounded in a batch process using a glass lined stirred reactor which is equipped with a jacket for cooling/heating, bottom drain valve, condenser, thermowell, and a nitrogen sparge. Methylene chloride (2500 g) is charged to the reactor followed by 4,4′-Oxydibenezenesulfonyl Azide (DPO-BSA) (250.00 g), IRGANOX® I-1010 (tetrakis-(Methylene (3,5-di-t-butyl-4-hydroxyhydrocinnamate))) (825.0 g), and IRGANOX® I-1076(octacecyl-3-(3,5-di-tert.butyl-4-hydroxyphenyl)-propionate) (349.02 g), stirring commenced and the temperature is raised to 81° C. resulting in a clear solution. Methylene chloride is taken overhead under vacuum from the mixture till a clear melt results at 93° C. When the batch is dry, the compounded polymer additive formulation is kept at 96° C. and poured into a stainless steel pan (32×18×4 inches), and allowed to cool to 25° C., then ground in a Franklin Miller grinder to obtain particles in the range of 200 to 2000 microns. The product was then dried in a vacuum oven at 40° C./1.0 mm Hg. The product is a free flowing powder which is not shock sensitive and can be handled with no special precautions. Analysis by HPLC shows the composition of this molecular melt to be 17.56 wt. % DPO-BSA, 57.93 wt. % IRGANOX® I-1010 and 24.51 wt. % IRGANOX® I-1076. Differential scanning calorimetry analysis determined that the DPO-BSA:I-1010:I-1076 molecular melt formed by this procedure exhibited a total crystallinity of 24.7% weighted average weight percent. FIG. 20 shows the differential scanning calorimetry results for Molecular Melt Sample L. One of ordinary skill in the art can determine from FIG. 20 that the bulk of the I-1076 is crystalline, whereas the DPO-BSA and I-1010 are amorphous in this molecular melt.

[0152] It is believed that a molecular melt comprised of DPO-BSA, I-1010 and I-1076 when reacted with a target polymer produces a more uniform coupled product, having lower gel count when made into a cast film. Additionally, this molecular melt advantageously exhibits the highly amorphous nature of a typical high amorphous DPO-BSA:I-1010 molecular melt, but also exhibits increased resistance to agglomeration, thereby reducing any blocking of the -molecular melt as compared with a typical high amorphous DPO-BSA:I-1010 molecular melt.

Example 15 Production of Rheology Modified Polymer using a DPO-BSA:I-1010 in a 1:3.3 Weight Ratio (1:1.066 Molar Ratio) Molecular Melt (Polymer Sample D)

[0153] Unless indicated otherwise, the base polypropylene used to make the samples used in all the following examples is isotactic polypropylene pellets, available from The Dow Chemical Company under the designation DC 108 PP. DC 108 is an impact copolymer of propylene with about 9 weight percent polymeric units derived from ethylene and a melt flow rate (MFR)=0.8 dg/min at 230° C./2.16 kg. DC 108 was coupled with a sufficient quantity of DPO-BSA: I-1010 in a 1:3.3 weight ratio molecular melt to provide 180 ppm of 4,4′-oxy-bis-(sulfonylazido)benzene (based on the total weight of the polymers present) to produce Polymer Sample D. The final melt flow rate of Polymer Sample D is 0.4 dg/min.

Example 16 Modifying Agent Molecular Melt Preparation Process Lab Preparation of Glass Mixture Between 4-Carboxybenzenesulfonazide (CBSA) and Irganox-1010 (CBSA/MM)

[0154] 54 grams of 4-Carboxybenzenesulfonazide [CAS 17202-49-2] and 54 grams of I-1010 were added to a two liter Rotovap vacuum distillation apparatus. Approximately 900 ml of methanol was added to the flask. All materials went into solution at room temperature. The flask was attached to a Rotovap brand vacuum distillation apparatus and slowly heated to 42 degrees Celsius and after one hour a slowly increasing vacuum was applied until a full vacuum was achieved. It took three hours to achieve a full vacuum and the flask was maintained at full vacuum at 42 degrees Celsius for another three hours. The product CBSA/MM was removed from the flask and placed in a sample bottle. A total of 105 grams of free flowing powder was obtained.

Example 17 Process to Manufacture High Molecular Weight Functionalized Polypropylene using CBSA/MM

[0155] Equipment: Leistritz 18 mm co-rotating twin screw extruder having an intensive mixing screw blanketed with nitrogen flow.

[0156] Materials:

[0157] Base resin: DC 108 MFR=0.8, impact copolymer available from The Dow Chemical Company.

[0158] Antioxidant: All the functionalized polymers made for this example have 2000 ppm Irganox B225 (available from Ciba Specialty Chemicals Company) in addition to the I-1010 introduced with the CBSA/MM. The B225 was tumble blended with the DC 108 and this mixture was added to the extruder in a separate stream from the CBSA/MM powder mixture described below.

[0159] Powder mixture: CBSA/MM was placed in a plastic bag and mixed with Profax 6501 (homopolymer polypropylene, 4 Melt Flow Rate) to form a powder master batch used for introducing the CBSA/MM into the reactive extruder for reaction with the DC 108.

[0160] The CBSA/MM used to prepare the functionalized polymers was that prepared in Example 16.

[0161] The following extrusion conditions, as shown in Table 3, were used for making the functionalized polypropylene (Polymers E1-E4). TABLE 3 Extrusion Temperature profile (° C.): Melt Zone 1 Zone 2 Zone 3 Zone 4 Zone 5 Die temp (° C.) (° C.) (° C.) (° C.) (° C.) (° C.) (° C.) 150 190 220 230 230 220 230

[0162] Observations during the reactive extrusion:

[0163] Torque decreases with increasing CBSA/MM concentration (see Table 4).

[0164] Pressure stayed about the same throughout each run.

[0165] Melt temperature stayed about the same throughout each run.

[0166] These results show a stable extrusion-process with little evidence of resin degradation. TABLE 4 Torque Polymer Torque (m-g) Polymer E1   4000 Polymer E2 ˜3800 Polymer E3 ˜3600 Polymer E4   3000

[0167] Gel permeation chromatography (GPC) analysis indicates significant retention of molecular weight for the functionalized polymers (Table 5). All the functionalized polymers of Table 5 were made by reacting the indicated amount of CBSA/MM with DC 108. The molecular weight does not change much as the concentration of CBSA used to functionalize the polymer changes from 2000 ppm to 23,000 ppm. The retention of molecular weight in a functionalized polymer is very advantageous and in stark contrast to functionalized polymers made using free radical grafting technologies. TABLE 5 Gel Permeation Chromatography CBSA (from Polymer CBSA/MM) Mw Mn Mw/Mn DC 108   0 ppm 442,600 100,200 4.42 Polymer E1  2000 ppm 397,400  89,900 4.42 Polymer E2  5000 ppm 385,300 100,900 3.82 Polymer E3 15000 ppm 370,100  93,400 3.96 Polymer E4 23000 ppm 401,700 104,300 3.85

Example 18 Use of Modifying Agent as a Compatibilizer for Nanoparticle Filled Propylene Based Polymers

[0168] Nanoparticle filled polymers are defined as particle filled polymers for which at least one dimension of the fundamental particle size is in the nanometer (10⁻⁹ m) range. Typically, polypropylene filled with nanoparticles are prepared when the polypropylene and filler are melt compounded in the presence of a compatibilizer, such as maleic anhydride grafted polypropylene (MAH-g-PP). The presence of compatibilizer is essential to achieve adequate dispersion and interfacial adhesion of the silicate layers. The anhydride group attached to the polypropylene chain promotes interfacial adhesion of the compatibilizer and the nanoparticle. The compatibilizer is designed to be miscible with the matrix. Thereby, assisting the dispersion of the nanoparticle in the matrix (in our examples DC 108 and/or Polymer Sample D). In Examples 18 and 19 a quaternized fluoromica (QFM), which was prepared by the ion exchange of a synthetic layered silicate (available from Coop Chemical, Japan, under the trade name Somasif ME 100) with a quaternary ammonium chloride (Arquad 2HT) was used. Additionally, maleic anhydride modified polypropylene (PP-g-MAH) available from Eastman Chemical Company under the trade name G3003 was used as a comparative compatibilizer.

[0169] The nanoparticle filled materials were prepared using the following zone temperature settings: Zone 1: 160° C., Zone 2: 180° C., Zone 3: 190° C., Zone 4: 200° C. and Die: 200° C. extrusion was carried out in a Werner & Pfleiderer co-rotating Twin Screw Extruder (ZSK30).

[0170] The nanoparticle filled polymer samples were injected molded into molds suitable for later testing according to ASTM defined test conditions. The samples were molded using a DeMag 100 Injection Molding machine having a 38 mm screw. The following zone temperature settings were used in the injection molding operation: Nozzle Zone: 430° C., Zone 3: 440° C., Zone 2: 420° C., Zone 1: 400° C.

[0171] Results:

[0172] Nanofilled samples having a 4-5 weight percent inorganic ash content were prepared in a DC 108 matrix and a Polymer Sample D matrix using Polymer E4 and PP-g-MAH as compatibilizers. The results are listed in Table 6 and graphically shown in FIG. 21. TABLE 6 Nanoparticle Filled Polymer Samples Nanoparticle filled polymer Examples A B C D E F Polypropylene Polymer Polymer DC108 Polymer DC108 Polymer Resin Sample D Sample D Sample D Sample D Resin wt % Filler QFM QFM QFM QFM QFM QFM Ash wt %  5.5  5.02  4.43  5.8  5.9  8.6 Compatibilizer PP-g-MAH PP-g-MAH Polymer Polymer E4 Polymer E4 Polymer E4 E4 Compatibilizer wt  10  5  5  5  5  5 % Flex Modulus (kpsi) 264 263 254 272 289 334 RT Notched Izod (ft  1.1  1.8  11.9  8.5  7.9  3.8 lb/in)

[0173] The toughness/stiffness balance for the nanoparticle filled polymer samples is shown graphically in FIG. 21.

[0174] In the case of Nanoparticle filled PP, this figure shows that Nanoparticle filled polymer using Polymer E4 as compatibilizer has a very much improved toughness/stiffness balance vs a similarly loaded system based on PP-g-MAH as compatibilizer.

Example 19 Adhesion of Functionalized Polymer Systems for Metals and Other Substrates

[0175] The Polymer E4, along with unmodified DC 108 was compression molded against aluminum foil. The aluminum foil was 0.26 mm thick and compression molded polymers were 0.6 mm thick. Samples were cut into 1″ wide strips and tested for adhesion.

Sample Preparation of the CBSA/MM Modified Samples for Adhesion Measurement

[0176] Equipment:

[0177] Carver automatic hydraulic hot press, model #4095-4PR1001.

[0178] Molding Procedure Used for the DC 108 and Polymer E4:

[0179] 1^(st) Molding Step:

[0180] 1. A “sandwich” made from the bottom up: holding tray, molding plate, mylar, 9″×9″×030″ chase, 40 g resin, mylar, and another molding plate, was placed in between platens 1 and 2 of the press for the following conditions: 218° C. 2 min.  2,000 lb. pressure 218° C. 2 min. 10,000 lb. pressure

[0181] 2. The tray was removed and placed in between platens 3 & 4 and cooled as follows: 35° C. 2 min. 2,000 lb. pressure

[0182] 3. The tray was removed and the molded/cooled plaque ˜6″×6″×0.0500″ was cut out of the chase.

[0183] 2^(nd) Molding Step:

[0184] 1. The molded plaque from the 1^(st) molding step above was placed into another “sandwich” configuration as described from the bottom up as a holding tray, molding plate, mylar, 9″×12″×0.030″ chase, the molded plaque, a 2″×6″ piece of mylar placed in the middle of the molded plaque, ˜6″×9″×0.130″ aluminum, and another molding plate on top.

[0185] 2. The tray was put into platens 1 and 2 of the press and molded as follows: 218° C. 2 min. 10,000 lb. Pressure

[0186] 3. The tray was removed and placed in between platens 3 and 4 of the press and cooled as follows: 35° C. 2 min. 1,000 lb. pressure

[0187] 4. The tray was removed from the press and the aluminum, 2″×6″ piece of mylar and the molded plaque were cut from the chase and kept together.

[0188] The samples were cut into one-inch wide strips, the polymer layer was initially separated from the aluminum layer using a razor blade and the initially separated layers placed into the jaws of an Instron testing machine. Adhesion was measured by pulling the samples in a 180° “T-peel” configuration (laminate horizontal, separated layers vertical) at a rate of 2 inches/minute. The results (average of five measurements) are shown in Table 7.

[0189] For the base resin (DC 108) there was no adhesion to the aluminum foil (i.e. the layers separated without any external force being applied) so adhesion level was recorded as zero g/in. In the case of Polymer E4 adhesion to aluminum is shown in Table 7. TABLE 7 adhesion to aluminum foil Avg Adhesion (g/in) 2059 Std Dev Adhesion 194 (g/in) Avg Adhesion (N/in) 20.2 Std Dev Adhesion 1.9 (N/in) Avg Adhesion (lb/in) 4.53 Std Dev adhesion 0.42 (lb/in)

[0190] While the above example specifically illustrates the use of CBSA as a modifying agent for polypropylene, other polar functional groups, such as hydroxyl, epoxy, anhydride, etc, linked to polypropylene (and other polymers) using the modifying agent molecular melt of our invention will also provide significant adhesive properties, which vary depending on the chemical properties of the functional group.

Examples 20-24 Polymers Modified With Modifying Agents and Coupling Agents For Wire & Cable Applications

[0191] The modifying agents of the present invention are useful for functionalizing polymer compounds used to coat wires and cables. In addition to the modifying agents, the wire and cable compounds may comprise one or more other additives, including but not limited to flame retardants, antioxidants, metal deactivators, plasticizers, lubricants, processing aids, antistatic agents, impact strength modifiers, fillers and reinforcements, fibers, blowing agents, carbon black, colorants, UV stabilizers, peroxides, and nucleating agents. Wire and cable compounds comprising inorganic additives, such as flame retardants, are found to exhibit improved mechanical properties when a polymer modified with CBSA/MM is present, when compared to the same formulations without the CBSA/MM modified polymer. Such compounds are useful as insulation, jacketing, buffer tube, or core tube applications for wire and cable. Furthermore, the coupling agents of the present invention can be advantageously used to make crosslinked insulation surrounding a conductor. The following non-limiting Examples 20-24 are intended to be illustrative. While Examples 20-24 mention specific polymers to be used, it is recognized that various polymers and polymer blends could be used as base resins or for modification with modifying agents and/or coupling agents for wire and cable applications. For example, homopolymer of propylene, random copolymers of propylene and other alpha-olefins, other impact propylene copolymers, ethylene vinyl acetate (EVA) based resins, homopolymer and copolymers of ethylene, EPDM, ethylene ethyl acrylate (EEA), ethylene styrene interpolymer (ESI) based polymers, and ethylene styrene propylene interpolymers (ESPI) based polymers may be used either modified or unmodified in the wire and cable compounds.

Example 20 CBSA/MM Modifying Agent in a Flame Retardant Wire Insulation Compound

[0192] To a Banbury mixer are added 10 pounds of magnesium hydroxide, two pounds of Polymer E4 from Example 17, and 28 pounds of DC 108 propylene based polymer. The mixture is raised to 190° C., at which temperature mixing is continued for three minutes. The mixture is then pelletized to form cable insulation compound A, which is then extruded around a preheated 18 AWG (American Wire Gauge) copper wire using a conventional extruder and conventional extrusion techniques, to form an insulated wire—“insulated wire A”—having an insulation thickness of 0.016 inches. A second compound is made under the same conditions in-the Banbury mixer by adding 10 pounds of magnesium hydroxide, one pound of as tetrakis [methylene (3,5-di-t-butyl-4-hydroxyhydrocinnamate)], and 29 pounds of DC 108 propylene based polymer, and pelletized to form cable insulation compound B, which is then extruded around a preheated 18 AWG copper wire using a conventional extruder and conventional extrusion techniques, to form an insulated wire—“insulated wire B”—having an insulation thickness of 0.016 inches.

[0193] The cable insulation compounds A and B are carefully stripped from their conductors and tested on an Instron tensile tester to determine the percent elongation at break. Stripping of the insulation is achieved by removing small portions of insulation to expose copper wire at both ends of a length of insulated wire, then grasping each exposed wire end with pliers and stretching the copper wire. After stretching the wire, the insulation can easily be slid off the conductor without damage, and subjected to the tensile test. Insulation from insulated wire A, which contains the CBSA/MM modified PP (Polymer E4), is found to have significantly higher tensile strength at break (as well as improvement in other physical properties) compared to insulation from insulated wire B.

Example 21 Modification of Insulation Adhesion to a Copper Conductor

[0194] To a Banbury mixer are added two pounds of the Polymer E4 from Example 17, and 38 pounds of DC 108 propylene based polymer. The mixture is then raised to 190° C. at which temperature it is mixed for three minutes. The mixture is then pelletized to form cable insulation compound C, which is then extruded around a preheated 16 AWG copper wire using a conventional extruder and conventional extrusion techniques, to form an insulated wire—“insulated wire C”—having an insulation thickness of 0.014 inches.

[0195] To a Banbury mixer are added one pound of as tetrakis [methylene (3,5-di-t-butyl-4-hydroxyhydrocinnamate)] and 39 pounds of DC 108 propylene based polymers. The mixture is then raised to 190° C. at which temperature it is mixed for three minutes. The mixture is then pelletized to form cable insulation compound D, which is then extruded around a preheated 16 AWG copper wire using a conventional extruder and conventional extrusion techniques, to form an insulated wire—“insulated wire D”—having an insulation thickness of 0.014 inches.

[0196] Insulated wires C and D are evaluated to measure the quality of adhesion of the insulation to the conductor using the procedure described in ASTM D4565. It is found that compound C exhibits a higher level of adhesion to the conductor than compound D, due to the presence of the carboxy groups from the CBSA.

Example 22 Flame Retardant Jacket Compound and Flame Retardant Cable

[0197] A polymer modifier, PE-CBSA1, is prepared by treating high pressure low density polyethylene (LDPE, density of 0.92 g/cc and melt index of 2.0 g/10 min.) with 23,200 ppm of CBSA/MM using similar conditions as in Example 17, except substituting the LDPE for the DC 108.

[0198] To a Banbury mixer are added two pounds of PE-CBSA1, 18 pounds of ethylene vinyl acetate copolymer (28% VA, 5.0 g/10 min. melt index), one pound of a masterbatch containing 40% of an N-110 type furnace carbon black (masterbatch carrier resin=EVA comprising 28% VA with a 5.0 g/10 min. melt index), 19 pounds of aluminum trihydrate, and 0.40 pounds of a 1:1 mixture of as tetrakis [methylene (3,5-di-t-butyl-4-hydroxyhydrocinnamate)] and distearylthiodipropionate. The mixture is then raised to 170° C. at which temperature it is mixed for three minutes. The mixture is then pelletized to form cable jacket compound A, which is then extruded around a core containing 2 twisted pairs of insulated wire A from above to form a cable with a 0.075 inch-thick jacket having excellent physical properties that result from the presence of PE-CBSA1.

Example 23 Crosslinked Insulation Made Using a Coupling Agent

[0199] To a Banbury mixer are added 39 pounds of LDPE (density of 0.92 g/cc and melt index of 2.0 g/10 min.) and one pound of the DPO-BSA molecular melt from Example 7. The mixture is raised to 140° C., at which temperature mixing is continued for three minutes. The mixture is then pelletized to form crosslinkable cable insulation compound E, which is then extruded around a preheated 18 AWG copper wire at a maximum extruder temperature of 140° C. using a conventional extruder and conventional extrusion techniques, to form an insulated wire—“insulated wire E”—having an insulation thickness of 0.016 inches. After exiting the extruder, the insulated wire is passed through a continuous vulcanizable steam tube wherein the surface temperature of the insulation reaches a temperature of about 200° C., and crosslinking occurs. Decalin extraction on the finished insulation verifies that the insulation contains a significant gel fraction.

Example 24 Grafted Acid Catalyst for Moisture Crosslinkable Insulation

[0200] To a Banbury mixer are added 37 pounds of a low density copolymer of ethylene and vinyl triethoxysilane, and three pounds of PE-CBSA1 of Example 22. The mixture is raised to 160° C., at which temperature mixing is continued for three minutes. The mixture is then pelletized to form a moisture crosslinkable cable insulation compound F, which is then extruded around a preheated 16 AWG copper wire at a maximum extruder temperature of 160° C. using a conventional extruder and conventional extrusion techniques, to form an insulated wire—“insulated wire F”—having an insulation thickness of 0.020 inches. Insulated wire F is then stored under ambient conditions for one week, during which time moisture from the atmosphere, catalyzed by the grafted carboxylic acid group, causes crosslinking. Decalin extraction on the insulation verifies that the insulation contains a significant gel fraction. This Example demonstrates that a carboxylic acid group added to a polymer by way of the modifying agent of the invention can serve as a catalyst to catalyze chemical reactions, such as the moisture curing of the crosslinkable cable insulation compound of this Example 24.

Examples 25-31 Salts of Modifying Agents, Molecular Melts Made from Such Salts, and Polymers Made Using Salts of Modifying Agents

[0201] The following Examples 25-31 illustrate Molecular Melt compounds containing salts of a modifying agent. It is believed that making such a salt prior to using it to modify a polymer will result in a process for making ionomeric polymers (i.e. polymers that have a small number of covalently bound charged groups attached to the backbone of the polymer), which is much more efficient and cost effective than currently available methods.

Example 25 Preparation of Zn⁺² Salt of P-Carboxybenzene Sulfony Azide

[0202]

[0203] The following description sets forth the reaction described in the above equation. A solution of 2.00 g of p-carboxybenzene sulfonyl azide (8.80 mmol) in 15 mL tetrahydrofuran (THF) was prepared in a dry-box. The solution was cooled to −40° C. (some of the azide precipitates) and treated with a cold solution of ZnEt₂ (4.4 mL, 4.4 mmol) in hexanes. After about 0.5 mL of the ZnEt₂ solution was added a brown solution formed, followed by a brown suspension as further solution was added. The suspension was allowed to warm to room temperature, stirred for 30 min, and evaporated. Analysis by Carbon-13 Nuclear Magnetic Resonance (¹³C NMR) (DMSO-d₆) gave resonances at 165.8, 140.9, 136.8, 131.0, and 127.8. The sample was analyzed using DSC (differential scanning calorimetry) in a aluminum pan (covered but not crimped) at a 10° C./min heating rate. An exotherm maximum of 189° C., onset at 130° C. with 771 J/g was observed.

Example 26 Preparation of a Molecular Melt from I-1010 and The Azide Salt From Example 25

[0204] The Zn⁺² salt (2.15 g, 4.15 mmol) from Example 25 was dissolved in 60 mL methanol with heating and treated with Irganox I-1010 (6.45 g, 5.26 mmol). The solvent was then evaporated using a rotary evaporator and a water bath thermostated to 80° C. A light-tan powder resulted (7.57 g). A light-tan powder resulted (5.22 g). Analysis by DSC revealed an exotherm maximum of 190° C., onset at 137° C. with 155 J/g, along with a small melting endotherm at 45° C. (4.2 J/g).

Example 27 Preparation of Na⁺ Salt of P-Carboxybenzene Sulfonyl Azide

[0205]

[0206] The following description sets forth the reaction described in the above equation. A solution of 1.00 g of p-carboxybenzene sulfonyl azide (4.40 mmol) in 5 mL THF was prepared in a dry-box. The solution was removed from the box, and treated with solid NaOH (0.176 g, 4.40 mmol) and 1.0 mL water. After stirring at room temperature, the solvents were evaporated in a stream of nitrogen. The pale-yellow solid was placed in a vacuum oven at 40° C. for 2 hours to give 1.13 g product. Analysis by DSC revealed an exotherm maximum of 178° C., onset at 145° C. (1062 J/g).

Example 28 Preparation of a Molecular Melt from I-1010 and The Azide Salt From Example 27

[0207] The Na⁺ salt (1.00 g, 4.01 mmol) from Example 27 was dissolved in 20 mL methanol with heating and treated with Irganox I-1010 (4.92 g, 4.01 mmol). The solvent was then evaporated using a rotary evaporator and a water bath thermostated to 80° C. A light-tan powder resulted (5.38 g). Analysis by DSC revealed an exotherm maximum of 189° C., onset at 133° C. with 184 J/g, along with a small melting endotherm at 116° C. (7.3 J/g).

Example 29 Preparation of Li⁺ Salt of P-Carboxybenzene Sulfonyl Azide

[0208]

[0209] The following description sets forth the reaction described in the above equation. A solution of 1.00 g of p-carboxybenzene sulfonyl azide (4.40 mmol) in 10 mL THF was prepared in a dry-box. The solution was cooled to −40° C. and treated with a cold solution of nBuLi (1.6M, 2.75 mL, 4.40 mmol) in hexane. After all of the nBuLi was added the yellow suspension was removed from the dry-box and evaporated. The pale-yellow solid was placed in a vacuum oven at 40° C. for 2 hours to give 1.12 g product. Analysis by DSC revealed an exotherm maximum of 186° C., onset at 126° C. (885 J/g).

Example 30 Preparation of a Molecular Melt from I-1010 and The Azide Salt From Example 29

[0210] The Li⁺ salt (0.96 g, 4.12 mmol) from Example 29 was dissolved in 20 mL methanol with heating and treated with Irganox I-1010 (4.72 g, 3.85 mmol). The solvent was then evaporated using a rotary evaporator and a water bath thermostated to 80° C. A light-tan powder resulted (5.22 g). The sample was analyzed using DSC (differential scanning calorimetry) in a aluminum pan (covered but not crimped) at a 10° C./min heating rate. Analysis by DSC revealed an exotherm maximum of 189° C., onset at 134° C. with 112 J/g, along with a small melting endotherm at 111° C. (12 J/g).

Example 31 Grafting of Azide Salts with Polypropylene

[0211] Each of the molecular melts from Examples 26, 28, and 30 (3.63 g of molecular melt from Example 30: 3.88 g of molecular melt from Example 28: 3.90 g of molecular melt from Example 26) were tumbled in separate batches with I000 g homopolymer polypropylene (Montell H-700-12) and 0.50 g B225 antioxidant. The concentrations were designed to give 1000 ppm CBSA. Each of the samples was extruded using a Werner and Pfleiderer ZSK-30, 30 mm twin screw extruder along with an Accurate Loss-in-Weight feeder resting on a scale. The feed rate was adjusted to 30 lbs/hr. The exit strand was chopped using a Sheer SWGS50-E pellitizer. The extruder speed was adjusted to 300 RPM, and the zones were set to 235° C. A grafted polypropylene product resulted. It is believed these ionomeric propylene based polymers will be relatively transparent and exhibit improved toughness and melt strength while maintaining the modulus/stiffness of the base polymers they are made from.

Example 32 Triazido Triamino Phosphazene (TTAP) Melt Blend Compounding Process to Manufacture TTAP:I-1010 in a 1.0:3.1 Weight Ratio (1:1 Molar Ratio) Molecular Melt

[0212] Diazido tetraphenoxy phophazene (Me₂N)₃(N₃)₃(PN)₃ is synthesized according to the method described by Allcock, et al (Inorganic Chem., 1999, 38, 5535-5544) from hexachlorophosphazene, dimethylamine, and sodium azide. It contains a small proportion of monoazide and bisazide. The triazide TTAP is compounded in a batch process using a glass lined stirred reactor which is equipped with a jacket for cooling/heating, bottom drain valve, condenser, thermowell, and a nitrogen sparge. Methylene chloride (4130 g) is charged to the reactor followed by TTAP (235.9 g, 0.600 mol) and IRGANOX® I-1010 (735.4 g, 0.600 mol), stirring commenced and the temperature is raised to 88° C. resulting in a clear solution. Methylene chloride is taken overhead from the mixture till a clear melt results at 94° C. The reactor is sealed and evacuated as the temperature is raised to 97° C. while methylene chloride (4022 g) is collected from the overhead (1.5 hours) and is recovered for recycle. A subsurface nitrogen sparge is used in the final hour to aid in removing the methylene chloride. When the batch is dry, the compounded polymer additive formulation is kept at 97° C. and poured into a pan (32×18×4 inches), cooled to 25° C., and ground in a Franklin Miller grinder to obtain particles in the range of 200 to 2000 microns. The product was then dried in a rotary drier at 40° C./10 mm Hg.

Example 33 Diazido Tetraphenoxy Phosphazene (DTPP) Melt Blend Compounding Process to Manufacture DTPP:I-1010 in a 1.0:2.1 Weight Ratio (1:1 Molar Ratio) Molecular Melt

[0213] Diazido tetraphenoxy phophazene (PhO)₄(N₃)₂(PN)₃ is synthesized according to the method described by Allcock, et al (Inorganic Chem., 1999, 38, 5535-5544) from hexachlorophosphazene, sodium phenate, and sodium azide. It is a mixture of cis-trans isomers, and contains a small proportion of monoazide and trisazide. The diazide DTPP is compounded in a batch process using a glass lined stirred reactor which is equipped with a jacket for cooling/heating, bottom drain valve, condenser, thermowell, and a nitrogen sparge. Methylene chloride (4130 g) is charged to the reactor followed by DTPP (354.8 g, 0.600 mol) and IRGANOX® I-1010 (735.4 g, 0.600 mol), stirring commenced and the temperature is raised to 88° C. resulting in a clear solution. Methylene chloride is taken overhead from the mixture till a clear melt results at 94° C. The reactor is sealed and evacuated as the temperature is raised to 97° C. while methylene chloride (4022 g) is collected from the overhead (1.5 hours) and is recovered for recycle. A subsurface nitrogen sparge is used in the final hour to aid in removing the methylene chloride. When the batch is dry, the compounded polymer additive formulation is kept at 97° C. and poured into a pan (32×18×4 inches), cooled to 25° C., and ground in a Franklin Miller grinder to obtain particles in the range of 200 to 2000 microns. The product was then dried in a rotary drier at 40° C./10 mm Hg. 

We claim:
 1. A method for making a modified polymer comprising the steps of: (a) mixing a molecular melt containing a modifying agent with a polymer; and (b) reacting the molecular melt with the polymer.
 2. The method of claim 1, wherein the reacting is caused by heating the molecular melt and the polymer.
 3. The method of claim 2, wherein the method is carried out in a mixer that mixes the molecular melt and polymer and provides sufficient heat to cause reaction between a modifying agent of the molecular melt and the polymer.
 4. The method of claim 3, wherein the method is carried out in a polymer extruder.
 5. The method of claim 1, wherein the modifying agent is a sulfonyl azide.
 6. The method of claim 3, wherein the molecular melt is comprised of an antioxidant selected from the group consisting of phenolic compounds and derivatives thereof, hindered amines and derivatives thereof, amine hydroxides and derivatives thereof, thioester compounds and derivatives thereof, hindered phenolic compounds and derivatives thereof, lactones and derivatives thereof, and mixtures thereof.
 7. The method of claim 3, wherein the modifying agent is selected from the group consisting of sulfonyl azides, phosphazene azides, silyl azides, formyl azides, azides, and mixtures thereof.
 8. The method of claim 6, wherein the antioxidant is tetrakis [Methylene (3,5-di-t-butyl-4-hydroxyhydrocinnamate)] or derivatives thereof and wherein the modifying agent is p-carboxybenzene sulfonyl azide or derivatives thereof.
 9. The method of claim 1, wherein the polymer to be modified is a polyolefin.
 10. The method of claim 3, wherein the polymer to be modified is a propylene based polymer.
 11. The method of claim 1, wherein the antioxidant is tetrakis [Methylene (3,5-di-t-butyl-4-hydroxyhydrocinnamate)] or derivatives thereof and wherein the modifying agent is p-carboxybenzene sulfonyl azide or derivatives thereof.
 12. A polymer made according to the method of claim
 11. 13. A polymer made according to the process of claim
 1. 14. A wire and cable composition containing the polymer of claim
 12. 15. A cable made from the composition of claim
 14. 16. The cable of claim 15, wherein the modified polymer is contained within the jacketing of the cable.
 17. The cable of claim 15, wherein the modified polymer is contained within the insulation of the cable.
 18. A wire and cable composition containing the polymer of claim
 1. 19. A cable made from the composition of claim
 18. 